AvBaeyer
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Preparation of Benzyl Chloride
Benzyl chloride is a very useful and reactive alkylating agent in organic synthesis. I recently had a need for this compound in order to make a sample
of benzylamine for use as a synthesis intermediate. Recently I posted my results for the preparation of benzylamine using the Delepine reaction in
another thread [1]. I thought it might be useful to others that I post my experiences in making benzyl chloride.
Nearly all example methods for the preparation of benzyl chloride involve the chlorination of toluene with elemental chlorine followed by fractional
distillation to separate it from its more highly chlorinated congeners. Of course, the immediate downside of this approach in the home laboratory is
the generation and handling of chlorine in a safe manner. N-Chloroamides such as N-chlorosuccinimide (NCS) and trichloroisocyanuric acid (TCCA)
reacting with toluene have also found use in some cases. In fact, TCCA has been mentioned a number of times in this forum as a possible reagent for
the preparation of benzyl chloride from toluene. This latter approach may well be suitable but does require fairly specific conditions to be useful.
Finally, any method requiring toluene has the problem that toluene is no longer easily available in many jurisdictions, especially here in California.
Benzyl alcohol, on the other hand, is quite easily obtainable and as I show below is readily converted in high yield to benzyl chloride by simply
reacting with aqueous hydrochloric acid. This simple reaction was first published by J. F. Norris in 1907. The reaction as published uses 12M
hydrochloric acid, though readily available from various vendors, is not OTC like the 10M acid commonly available in hardware stores. So the question
became could OTC 10M hydrochloric acid be used in the Norris procedure with results comparable to the 12M acid. Three different experiments have been
run with 10M hydrochloric acid that show that it can work just as well as the 12M acid.
Experiment 1 is a direct repeat of the Norris procedure using reagent grade 12M hydrochloric acid. Experiment 2 was a first attempt at direct
replacement of 12M acid by 10M acid. In order to work properly, a small amount of 12M acid needed to be added to the reaction. Experiment 3 was an
attempt to “fortify” the 10M acid with sodium chloride and sulfuric acid. Although this experiment worked, the reaction of the sulfuric acid with
the hydrochloric acid was quite unpleasant even though everything was at ice bath temperature. Experiment 4 was a result of considering the outcomes
of experiments 1-3 and concluding that a greater amount of 10M acid would work fine which is what happened. Descriptions of these experiments follow.
NOTE: It is extremely important to use gloves, eye protection and a lab apron or coat during these experiments. Working in a well ventilated area or
out of doors is also necessary. Great care must be exercised in disposal of reaction waste and in washing of contaminated glassware. Benzyl chloride
is highly lachrymatory and can cause severe reaction upon contact.
Experiment 1: The Norris Procedure
12M Hydrochloric acid (60 ml, 0.72 mol) is added to benzyl alcohol (20.0 g, 0.185 mol) whereupon one obtains a clear solution. The reaction mixture is
slowly heated to 60C (oil bath) during which it becomes cloudy and an oil begins to separate at a bath temperature of about 50C. After about 20
minutes at 60C the reaction, which is now biphasic, is removed from the heating bath and cooled to ambient. The mixture is transferred to a separatory
funnel with the aid of hexanes (25 ml, use caution) [3] and the upper layer containing benzyl chloride isolated. The aqueous layer is extracted with
hexanes (1x25 ml) and combined with the first organic layer. The combined organic layers are washed (2x25ml water, 1x25ml 5% sodium bicarbonate and
2x25 ml brine) then dried over calcium chloride [3a]. Removal of the hexanes by distillation affords 21.7 g (92%) of a colorless product. Distillation
affords 19.4 g (83%, bp 51-52 C @ 5 mm) pure benzyl chloride. A small pot residue remains [4] as well as some hold up in the distillation apparatus
[5].
Experiment 2: 10M Hydrochloric acid with added 12M Hydrochloric acid.
10M Hydrochloric acid (60 ml, 0.60 mol) is added to benzyl alcohol (20.0 g, 0.185 mol) which gives incomplete solution. Heating was commenced but
incomplete dissolution was still present at 40C. At this point, 12M acid was added until dissolution was complete which required about 6 ml of acid.
When the bath temperature reached about 50C, there was immediate separation of an oil as in Experiment 1. From this point on, the same procedures as
in Experiment 1 were followed. Distillation afforded 15.08 g of benzyl chloride (64%, bp 52-54 C @ 4 mm). The pot residue tested positive for both
chloride and alcohol [4].
Experiment 3: 10M Hydrochloric acid with sodium chloride and sulfuric acid.
A mixture of 10M Hydrochloric acid (60 ml, 0.60 mol) and powdered sodium chloride (7.0 g, 0.12 mol) was well chilled in an ice bath. Concentrated
sulfuric acid (ca 18M, 6 ml, ca 1.0 mol) was added very cautiously with a dropper while stirring. This caused a vigorous reaction and considerable
ejection of HCl fumes. After warming to ambient temperature, benzyl alcohol (20 g, 0.185 mol) was added which appeared to completely dissolve [6].
From this point, the conditions of Experiment 1 were followed. Distillation afforded 20.38 g of benzyl chloride (87%, bp 77-79 @ 25 mm) [7]. The pot
residue was not tested.
Experiment 4: 10M Hydrochloric acid alone.
Benzyl alcohol (21.98 g, 0.203 mol) was added to 10M hydrochloric acid (100 ml, 1.0 mol) to give a clear solution. The reaction was slowly heated to
65 C. At 60 C there was an immediate cloudiness and separation of an oil. The reaction was maintained at 65 C for 1.5 hr then allowed to cool to room
temperature. Work up was as in Experiment 1. Distillation afforded 23.24 g of benzyl chloride (90%, bp 69-72 C @19 mm). The pot residue was not
tested.
The last three samples of distilled benzyl chloride gave negative tests with chromic acid reagent indicating no benzyl alcohol within the limits of
sensitivity of the test [8].
Conclusion
OTC 10M hydrochloric acid works remarkably well for converting benzyl alcohol to benzyl chloride. More acid and a longer reaction time relative to the
original Norris procedure using 12M hydrochloric acid may be the key variables for success.
[1] http://www.sciencemadness.org/talk/viewthread.php?tid=70913#...
[2] JF Norris, American Chemical Journal 1907, v38, 647-642.
[3] I use a distillation cut of Coleman fuel with bp 60-75 C.
[3a] About 12 g of calcium chloride was used for the drying. The hexane solutions stood over the drying agent for 18 - 24 hrs. The calcium chloride
was washed with 20-30 ml of hexanes in the filtration process. It was noted that the calcium chloride became quite "brittle" during the drying
process.
[4] The pot residue tested positive for chloride (ethanolic silver nitrate) and negative for alcohol (dilute chromic acid). It is most likely that
the major part of the residue is dibenzyl ether.
[5] All distillations were done using standard 14/20 glassware.
[6] Considerable solids were present in the reaction, presumably sodium chloride.
[7] At this point I switched to a recirculating aspirator pump as use of my vacuum pump did not seem like such a good idea.
[8] Shriner, Fuson and Curtin, “The Systematic Identification of Organic Compounds,” 1964 edition, page 125.
AvB
[Edited on 4-12-2016 by AvBaeyer]
[Edited on 4-12-2016 by AvBaeyer]
[Edited on 4-12-2016 by AvBaeyer]
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DJF90
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Nice work Av. One comment from me: Did you consider the use of calcium chloride or zinc chloride as catalysts for the reaction? Not that there is
anything wrong with your optimised procedure (except theres a typo in the quantity of acid - 100 mL is 1 mol).
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careysub
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This is very valuable information. Benzyl chloride is a reagent of many applications, and all but impossible to purchase. These procedures make it
readily available.
About that which we cannot speak, we must remain silent.
-Wittgenstein
Some things can never be spoken
Some things cannot be pronounced
That word does not exist in any language
It will never be uttered by a human mouth
- The Talking Heads
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kmno4
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Generally, it is nothing new, see for example this:
http://www.lambdasyn.org/synfiles/benzylchlorid.htm
However, exeptionally high yields are reported here.
I would suggest to check real purity of prepared BnCl by its hydrolysis and titration with NaOH and/or to check refractive index before and after 24
hours treatment with fresh CaCl2 (it removes BnOH).
Слава Україні !
Героям слава !
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Marvin
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This is really good work AvB. I actually bought toluene specifically to make benzyl chloride with, and was not looking forward to the attempt in the
least. I heard about the alcohol method and so far simply haven't got around to trying it. My home chemistry is on hiatus currently. This practical
description is very valuable to me.
The improved yields relative to the lambdasyn description may be due to the hexane extraction.
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Magpie
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Thank you AvB for this valuable contribution. I know how tedious and time consuming research can be. I'm currently in that situation myself, but
without your success.
The single most important condition for a successful synthesis is good mixing - Nicodem
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aga
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Superb quality post AvBaeyer.
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AvBaeyer
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Responses to comments
DJF90: Thank you for the typo sighting. It is corrected. I did not consider the use of either calcium chloride or zinc chloride in this reaction.
kmno4: I am making no claims to “new” chemistry. After all, the original procedure is over 100 years old. I am simply making fellow chemists aware
that benzyl chloride is easily available. Moreover, I am unaware of the lambdasyn website. Thank you for pointing this out.
I have today checked the purity of my products as best I can using qualitative analysis. Negative results were seen with chromic acid reagent which
rules out benzyl alcohol contamination though I do not know the lowest level of detection. The test was that described in Shriner, Fuson and Curtin,
“The Systematic Identification of Organic Compounds,” 1964 edition, page 125. I have also added a note in the edited procedure giving more detail
about the calcium chloride drying of the hexane extracts.
careysub, Marvin, Magpie and aga: Thank you for your comments- much appreciated.
AvB
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DDTea
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| Quote: | | OTC 10M hydrochloric acid works remarkably well for converting benzyl alcohol to benzyl chloride. More acid and a longer reaction time relative to the
original Norris procedure using 12M hydrochloric acid may be the key variables for success. |
In this particular molecule, there's no potential for eliminations or rearrangements. I don't see any potential for side reactions. So let it
reflux, forget about it, and check on it after a few days. Nothing to lose!
This is a good write up. Were you monitoring each of these experiments using the chromic acid test? If so, it would be interesting if you could
repeat this with some qualitative kinetics measurement. i.e.: how long until the first negative test?
I have an editorial critique: Could you make a tabular summary of your data?
Something like:
Experiment / benzyl alcohol (mmol) / Acid conc. / Acid mmol / Additives / Yield
1 / 185 / 12 M / 720 / none / 83%
2 ....
3....
4.....
You decide which parameters are important. But doing so will be helpful to readers.
"In the end the proud scientist or philosopher who cannot be bothered to make his thought accessible has no choice but to retire to the heights in
which dwell the Great Misunderstood and the Great Ignored, there to rail in Olympic superiority at the folly of mankind." - Reginald Kapp.
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Dr.Bob
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I recently ran a similar experiment with a substituted benzyl alcohol, and while I used 12 N HCl, I think most of these will go to a good degree with,
10N, it just shifts he equilibrium slightly to the left, so you either need more acid, or the yield is lower, or you can also use lower conc, and then
do two steps, react the first time, work it up, then use a fresh portion of acid to further drive the reaction to the right. That would allow you to
convert part of the alcohol in the first reaction, then extract the partially pure product with hexanes, then re-react the material with another
portion of acid.
I found that for my compound I got about 95% conversion the first time, and retreating it with HCl again, go it purer, to about 98%. In my case the
distillation would have been less practical, due to a higher MW. But sometimes doing two small amounts of acid can get you to the same level of
purity that one treatment with 10x as much would do in one reaction.
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chemplayer...
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Great work. We did this using 36% hydrochloric acid and with anhydrous zinc chloride added (Lucas' reagent). But you are getting just as good yields
if not better after distillation.
The problem with the zinc chloride method is that the exotherm created as the zinc chloride dissolves in the acid causes a lot of highly corrosive HCl
fumes to come off. Slow addition with cooling is needed.
Distillation is necessary for a pure product - the top layer of oily liquid which separates during the reaction does seem to contain appreciable
dissolved benzyl alcohol.
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Illegal Parkinson
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Where do you aspire that you are going with this synthesis?
The reaction of 2 equivalents with 1 equivalent of methylamine would give Dibemethine.
Fb: [102-05-6]
This was stated to have analgesic properties.
https://books.google.co.uk/books?id=0vXTBwAAQBAJ&pg=PA79...
A more challenging goal is to target Dibenamine.
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MrDoctor
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I was entertaining the idea of using calcium chloride, such as a brine or just a single fused chunk added mid-way, to re-concentrate the acid to move
things along because smaller glassware and less washing keeps the tears away, and although this should be obvious i thought i would just go and say
this anyway to anyone who might try it since i almost did it and didnt factor this in: after making benzyl chloride, prior to distillation you will
perform a seperation and washing.
if you use calcium chloride, when you neutralize the HCl, you will potentially gunk up your seperatory funnel with calcium carbonate that precipitates
out if enough is left in there, and the use of a co-solvent may make that worse. At very least a pure water wash is warranted i think prior to the
standard 2x bicarbonate and 1x brine. Still i cringe at the idea of having to wash out SOLIDS from the glassware afterwards, i just want to soak it
all in some cleaning solution in a great big tub and forget about it.
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Keras
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Quote: Originally posted by chemplayer...  | Great work. We did this using 36% hydrochloric acid and with anhydrous zinc chloride added (Lucas' reagent). But you are getting just as good yields
if not better after distillation.
The problem with the zinc chloride method is that the exotherm created as the zinc chloride dissolves in the acid causes a lot of highly corrosive HCl
fumes to come off. Slow addition with cooling is needed. |
Nice to see you again. We miss your vids!
Isn't benzyl bromide easier to prepare?
[Edited on 22-8-2024 by Keras]
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WFOnitroNerd
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Ok so quick question you state when you mixed otc hcl with benzyl alcohol it gave a clear solution and didn't give 2 layers until you heated when I
mixed my benzyl alcohol and OTC hcl I acquired 2 layers with the upper alcohol layer turning a ever so slight blue color I went ahead and refluxed it
but don't believe any benz chloride formed it's still cooling down but pretty sure what I'm aiming for didn't work any thing I could add that may
help nacl h2so4? And what is up with blue color wasnt expecting it to turn a light sky blue not as if any nox was in it ? What am I missing
[Edited on 26-9-2024 by WFOnitroNerd]
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clearly_not_atara
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Are you sure that your benzyl alcohol is pure? None of these compounds should be blue.
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Random
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What about SO2Cl2.
I saw a topic yesterday which I wrote... what it was. ?20i2
...
[Edited on 27-9-2024 by Random]
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WFOnitroNerd
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Benzyl alcohol is pure well from eBay made a liter of benzaldehyde with it. it is about a year old. this is the color change I get with it. It has me
super confused
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AvBaeyer
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How pure is your HCl? Is it some otc junk? Some otc HCl is essentially industrial waste sold as concrete cleaner. What is the concentration? It should
be at least 30 -32% (10M) to efficiently dissolve benzyl alcohol.
AvB
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WFOnitroNerd
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My hcl is OTC hardware Junk it has to be the issue cause the oh is of good quality imma try and extract it and add more hcl and reflux it again maybe
I should hit up drbob and get some goodies for the lab and then try it again
[Edited on 27-9-2024 by WFOnitroNerd]
[Edited on 27-9-2024 by WFOnitroNerd]
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AvBaeyer
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I should have mentioned that I get my otc HCl from the local ACE hardware store. It is 30-32% and colorless. Most importantly, evaporation of a few
mls (flame, outdoors) in a beaker leaves absolutely no residue. It is really clean material.
AvB
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MrDoctor
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| Quote: Originally posted by WFOnitroNerd | Ok so quick question you state when you mixed otc hcl with benzyl alcohol it gave a clear solution and didn't give 2 layers until you heated when I
mixed my benzyl alcohol and OTC hcl I acquired 2 layers with the upper alcohol layer turning a ever so slight blue color I went ahead and refluxed it
but don't believe any benz chloride formed it's still cooling down but pretty sure what I'm aiming for didn't work any thing I could add that may
help nacl h2so4? And what is up with blue color wasnt expecting it to turn a light sky blue not as if any nox was in it ? What am I missing
[Edited on 26-9-2024 by WFOnitroNerd] |
That blue color is titanium chloride. I think the color intensifies in "reducing conditions", whatever that means, ive just been told that it can
exist in some colorless form but as soon as another metal is introduced, or something else, it becomes its usual strong colored self. It might be
complexing with excess HCl or something so anything that takes that away restores it to default state. the addition of a base would most likely react
with the titanium chloride to, removing it, so it would only appear in conditions where you are depleting the HCl in a specific way.
Here is my attempt at extracting tin chloride from some expired SnPb solder paste. both began at the same concentration, there is a color shift that
occurs too which is concentration dependent.
I have no idea why it contains so much titanium however, unless it slightly reduces the fuming while maintaining the same effective HCl content, idk.
This is the cause of that indestructible white mess, as an oxychloride-dioxide mixture, when you distill HCl too far.
[Edited on 1-10-2024 by MrDoctor]
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