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Picric-A
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Quote: Originally posted by entropy51  | There is an OTC product which consists mainly of sodium dithionite and carbonate. I don't know about the luminol synthesis, but it works for a number
of other purposes.
Rit Color Remover http://www.ritdye.com/Fabric+Treatments.28.51.7.49.lasso
Dithionite can also be prepared by reducing SO2 with sodium formate in aqueous methanol. There is a reference posted around here somewhere on this
method.
[Edited on 17-9-2009 by entropy51] |
I have not found an OTC product containing Dithionite here in the UK.
As to the synthesis via reduction of methanol, there are lots of reperences and patents to that but i decided it only looked viable on an industrial
scale.
Attachment: sodium dithionite from formate + SO2.pdf (603kB)
This file has been downloaded 664 times
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entropy51
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| Quote: Originally posted by Picric-A |
As to the synthesis via reduction of methanol, there are lots of reperences and patents to that but i decided it only looked viable on an industrial
scale. |
Oh did you now?
I guess an amateur like myself shouldn't attempt it then?
It works in the lab if one has source of SO2.
You can also prepare an aqueous solution by stirring up NaHSO3 with Zn dust.
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Picric-A
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| Quote: Originally posted by entropy51 | | Quote: Originally posted by Picric-A |
As to the synthesis via reduction of methanol, there are lots of reperences and patents to that but i decided it only looked viable on an industrial
scale. |
Oh did you now?
I guess an amateur like myself shouldn't attempt it then?
It works in the lab if one has source of SO2.
You can also prepare an aqueous solution by stirring up NaHSO3 with Zn dust. |
I was not questioning your ability, i was meerly stating large reactors are needed, solutions containing mixtures of methyl formate, and lots of other
chemicals are needed as a reaction base (see lit.) followed by a cheap SO2 source (my only source is H2SO4 + Cu- i am going to buy a cylinder soon
though). Overall it seems like more trouble than its worth
I have given the NaHSO3 method a shot, but i didnt have powdered Zn, only granules. upon standing in a NaHSO3 solution for 24 hours, i got a
colourless solution with the lump of Zn in and a lot of white ppt in the bottom (Zn(OH)2).
Could be a good method however powdered Zn if definitly needed
[Edited on 18-9-2009 by Picric-A]
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1281371269
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Powdered Zn is dead easy to get. It was the first chemical I bought.
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Jor
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Garage chemist gas mentioned the anhydride of periodic acid (diiodine heptoxide) on this forum once. It is supposed to be an orange polymeric solid.
I added a spatula of periodic acid to 2mL of conc. H2SO4, and I then heated with a propane burner. The solid just dissolves, but no orange color is
produced.
I added 3mL of DCM and shook vigorously, I then took the DCM layer, and boiled away the DCM. No residue remained. My guess is that I2O7 should be
soluble in DCM, so no anhydride was formed.
Does anyone know how it can be synthesised? Without using things like oleum. Maybe heating periodic acid with phosphorus pentoxide?
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entropy51
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| Quote: Originally posted by Picric-A | | i was meerly stating large reactors are needed, solutions containing mixtures of methyl formate, and lots of other chemicals are needed as a reaction
base (see lit.) |
The patent you posted specifies a reactor because they're describing a large-scale industrial application of the reaction.
It works just fine in a stirred flask. You need only sodium formate, methanol and SO2.
The Zn reduction of NaHSO3 is even easier, but does require Zn dust.
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bbartlog
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What is produced at the anode if I electrolyze molten ammonium acetate (ammonia at the cathode, I expect)? Assume I use a PbO2 anode or the like,
making the formation of a metal acetate or the like from the anode material unlikely. I'm having trouble seeing what the C2H3O2 anion would turn into,
and the references I see online mostly talk about using ammonium acetate to assist in the electrolysis of something else (or turning it into
nanocrystalline diamond via unorthodox voltage and electrodes).
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ketel-one
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^interesting question. The way I imagine it is that the AcO* radical would do a hunsdiecker type thing and make CH3* + CO2, two of the CH3* combining
to make CH2CH2. Or it could make Ac-O-O-Ac, and decompose into something.
How do you know when an alcohol can be chlorinated with HCl? Is it correct that you can make tertiary halides from tertiary alcohols simply with HCl
at RT?
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UnintentionalChaos
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| Quote: Originally posted by bbartlog | | What is produced at the anode if I electrolyze molten ammonium acetate (ammonia at the cathode, I expect)? Assume I use a PbO2 anode or the like,
making the formation of a metal acetate or the like from the anode material unlikely. I'm having trouble seeing what the C2H3O2 anion would turn into,
and the references I see online mostly talk about using ammonium acetate to assist in the electrolysis of something else (or turning it into
nanocrystalline diamond via unorthodox voltage and electrodes). |
| Quote: Originally posted by ketel-one | ^interesting question. The way I imagine it is that the AcO* radical would do a hunsdiecker type thing and make CH3* + CO2, two of the CH3* combining
to make CH2CH2. Or it could make Ac-O-O-Ac, and decompose into something.
How do you know when an alcohol can be chlorinated with HCl? Is it correct that you can make tertiary halides from tertiary alcohols simply with HCl
at RT? |
Look up the Kolbe Electrolysis. I'm going to guess that you'd turn two NH4+ into 2 NH3 and a H2 at the cathode and perform the standard kolbe
electrolysis at the anode, forming ethane and CO2.
ketel-one A mixture of conc. HCl and zinc chloride is called Lucas's reagent and may be of some assistance here. Usually the reaction is done at
reflux to get good yields.
Department of Redundancy Department - Now with paperwork!
'In organic synthesis, we call decomposition products "crap", however this is not a IUPAC approved nomenclature.' -Nicodem
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ketel-one
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Many thanks Chaos, that explains everything.
Oh and that CH2CH2 should have been CH3CH3 obviously.
[Edited on 19-9-2009 by ketel-one]
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not_important
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| Quote: Originally posted by Jor | | Garage chemist gas mentioned the anhydride of periodic acid (diiodine heptoxide) on this forum once. It is supposed to be an orange polymeric solid.
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From Inorganic chemistry Egon Wiberg, Nils Wiberg, Arnold Frederick Holleman, 2001, comes the attached.
References from the 1990s talk about the heptoxide, mention it as orange, and state a very similar preparation to the hexoxide. Guess we need to find
some journal references.
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ketel-one
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Alkylation reactions have to be performed in nonpolar solvent right? A 40% aqueous alkyl halide would have to be distilled out first, yes?
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sonogashira
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No not really. I think it is better in a polar solvent in fact. But likely it depends on what you are alkylating. Phenols are alkylated with dimethyl
sulfate in water, alkyl halide in alcohols etc. (I have not heard of alkyl halide in water being used though - likely it is better to have it in
alcohol but it may work.) As I say it depends what you have to alkylate and the size of the alkyl group though. 
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woelen
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| Quote: Originally posted by not_important |
From Inorganic chemistry Egon Wiberg, Nils Wiberg, Arnold Frederick Holleman, 2001, comes the attached.
References from the 1990s talk about the heptoxide, mention it as orange, and state a very similar preparation to the hexoxide. Guess we need to find
some journal references. |
I have the book "Chemistry of the Elements" from Earnshaw and this tells that I2O7 does not exist. There is no anhydride of periodic acid. The
compound I2O6 certainly may exist, but I2O7 probably does not. The orange material, mentioned by Jor, probably is an impure compound, contaminated
with iodine, which can explain the orange color.
[Edited on 19-9-09 by woelen]
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Klute
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40% aqueous alkyl halide solution? What alkyl halide is soluble to the extent of 40% in water? Are you not confusing with the amine? Or a solution in
alcohol?
\"You can battle with a demon, you can embrace a demon; what the hell can you do with a fucking spiritual computer?\"
-Alice Parr
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ketel-one
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Lol, good point. I Must've had some unreacted alcohol.
Does anyone know... if you try to halogenate piperidine (or pyridine), would it halogenate at the 2 or the 4 position? Could iodine be used for that
purpose with acetone as solvent?
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Klute
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Pyridine will be halogenated to the 3 and 5 positions with difficulty, requiring hot temperatures. See p. 58 in the book "Preparation of organic
intermediates" that sonigasira posted in the aluminium alkoxide thread (org chem forum).
\"You can battle with a demon, you can embrace a demon; what the hell can you do with a fucking spiritual computer?\"
-Alice Parr
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sonogashira
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| Quote: Originally posted by ketel-one | Lol, good point. I Must've had some unreacted alcohol.
Does anyone know... if you try to halogenate piperidine (or pyridine), would it halogenate at the 2 or the 4 position? Could iodine be used for that
purpose with acetone as solvent? |
From Joule & Mills' Heterocyclic Chemistry:
"2-Bromo- and 2-chloropyridines can be made extremely efficiently by reaction of pyridine with the halogen, at 0-50C in the presence of palladium(II)
chloride[25]"
And reference 25 is attached.
4-position is via the N-oxide
Attachment: s-1980-29025.pdf (129kB)
This file has been downloaded 856 times
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Siddy
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Sorry to butt in...
Say a clumsy chemist was to break a piece of glassware, what is the best adhesive they should use?
I fixed the outlet on the water jacket of a condenser with cyanoacrylate which works perfectly, but what if you were repairing something that may come
into contact with organic solvents?
Cyanoacrylates are soluble in acetone, DCM etc.. before they set. (eg, directions on super glue says clean excess with acetone before dries).
Does anyone one if it will hold up once set, to at least acetone, hopefully DCM too?
Or is there a better adhesive to use?
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JohnWW
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Cyanoacrylate glue ("Superglue") is supposed not to work on materials containing alkalis, including soda glass. Two-pot epoxide glues - "Araldite" -
are supposed to be the appropriate glue for such materials.
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watson.fawkes
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| Quote: Originally posted by Siddy | | Say a clumsy chemist was to break a piece of glassware, what is the best adhesive they should use? |
It's
torch heat. Blow during and anneal afterward.
Really? If there were an adequate resin or polymer to repair glass, wouldn't there be labware made out it?—since it's cheaper to cast
plastic than to blow glass.
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Ephoton
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Mood: trying to figure out why I need a dark room retreat when I live in a forest of wattle.
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dont bother you broke it hehe you buy another simple.
post whoredom is mine whaa ha ha ha
e3500 console login: root
bash-2.05#
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Siddy
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Thanks JohnWW!
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Jor
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I'm currently doing the synthesis of 3-nitrophtalhydrazide. I added NaOH to a suspension of 2,11g 3-nitrophthalic acid until the solution turned pink
(phenolphthalein). i then added a pinch of 3-nitrophthalic acid to make it yellow again. I then added 1,35g (slight excess) of hydrazine sulfate, and
boiled the solution down to the point where a crystal crust formed. I then added about 15mL of glycerin, and heated the solution at 170-185C for 1
hour.
Now my first question is, at this point there was already quite some precitipate, while in the method on versuchschemie, a clear red liquid is
obtained. How is this possible? Might it be possible that phtalhydrazide or 4-nitrophthalhydrazide precitipated, because of impurities in the
3-nitrophthalic acid (i made this myself).
Next I made a very stupid mistake. I added water about 1,5x the volume, to the still 150C solution (I was impatient) and there was some boiling.
Now what i forgot is possible hydrolysis. Is it possible that at those temperatures a lot of my 3-nitrophthalhydrazide hydrolysed? How prone is a
hydrazid group to hydrolysis at slightly acidic pH?
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ketel-one
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| Quote: Originally posted by not_important |
You can use iodine, water, and H2S, which give aqueous HI and elemental sulfur; iodine, water, and SO2, which gives you aqueous HI and H2SO4; or I2,
H2O, and red phosphorous, the favorite of meth makers.
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I've thought of an easier way, (no sulfur or phosphorous required); iodine is extracted very easily from medicinal iodine, and it reacts very
violently with aluminum (you don't even need aluminum powder, just small squares cut with scissors out of aluminum foil); reaction starts
spontaneously, produces lots of heat, and should be contained or lots of iodine will vaporize. That's to get Al-I3.
Then what I'm thinking is:
Al-I3 + 33%HCl = AlCl3 + 63%HI
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