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P2P from recycled styrene? [quote][i]Originally posted by Sauron[/i]
There's a big difference between him and those of us who ... |
6-4-2007 at 03:01 by: Nicodem |
Frustrating Chemical Just for the record, the Houben-Hoesch reaction for preparing 2,4,6-trihydroxyacetophenone is featur ... |
5-4-2007 at 23:33 by: Nicodem |
Frustrating Chemical The reaction is called the [url=http://www.jergym.hiedu.cz/~canovm/mechanic/pravidl2/hoe/h.htm]Hoube ... |
5-4-2007 at 22:20 by: Nicodem |
Nitrobenzene The chlorine and other halogen substituents on benzene are ortho/para directing for electrophilic su ... |
5-4-2007 at 09:49 by: Nicodem |
Frustrating Chemical Why don't you use the usual method for preparing 2,4,6-trihydroxyacetophenone, the reaction of flour ... |
5-4-2007 at 00:44 by: Nicodem |
washes and extractions Heating the emulsion up to the boiling point of CH2Cl2 often efficiently breaks it (not always thoug ... |
5-4-2007 at 00:23 by: Nicodem |
Prep. of EtNO2 using acetone as solv. [quote][i]Originally posted by Furch[/i]
Sure, my common sense tells me that as well... But I also ... |
4-4-2007 at 23:28 by: Nicodem |
washes and extractions But at the stage of drying with Na2SO4, the hydrochloride salt is already formed and in solution? Al ... |
3-4-2007 at 23:16 by: Nicodem |
Benzoquinone from Paracetamol [quote][i]Originally posted by tupence_hapeny[/i]
My only interest is basically whether it is or is ... |
3-4-2007 at 09:57 by: Nicodem |
Using [Cu(Cl)4]2- to activate Al for reductions Well, actually if a compound gets consumed during the course of a reaction, then it can not be calle ... |
3-4-2007 at 00:38 by: Nicodem |
washes and extractions No, diethyl ether is anything but comparable to THF by its solvating properties.
Amine sulfates a ... |
3-4-2007 at 00:17 by: Nicodem |
reductive am. why inert atmosphere? Whether the inert atmosphere is truly necessary or not can not be answered without knowing what the ... |
3-4-2007 at 00:07 by: Nicodem |
washes and extractions Volumes? That is up to you. I can not answer you that.
No, bubbling HCl through the CH2Cl2 phase ma ... |
2-4-2007 at 00:09 by: Nicodem |
washes and extractions 1.) Yes it now makes sense.
2.) Just follow the instructions, the workup as it is, is just fine.
... |
1-4-2007 at 23:42 by: Nicodem |
Uses for acrylamide Ups, sorry, I was not thinking much about what the product was. You are right and it should have add ... |
1-4-2007 at 23:28 by: Nicodem |
washes and extractions I agree with Sandmeyer, but have to add a note of cautiousness that there are lots (well, relatively ... |
1-4-2007 at 14:01 by: Nicodem |
washes and extractions There is something terribly illogical in your extraction procedure.
Your substance is obviously pre ... |
1-4-2007 at 11:54 by: Nicodem |
Uses for acrylamide Well, a bunch of things are carcinogenic. Who cares except for the non-chemists?
Anyway, acrylamide ... |
1-4-2007 at 10:39 by: Nicodem |
n-methyl-3,4-Dihydroxyphenylalanine (orgsyn) I had no time to reply to some previous posts though I wanted to, so…
[quote][i]Originally posted ... |
1-4-2007 at 10:24 by: Nicodem |
Pyridine hydrogenation - methods? [quote][i]Originally posted by chemrox[/i]
[quote]NaBH4 only reduces quarternary pyridinum salts to ... |
1-4-2007 at 01:24 by: Nicodem |
n-methyl-3,4-Dihydroxyphenylalanine (orgsyn) Confusing lots of stuff again? It is getting a habit already. ![:)](./images/smilies/smile.gif)
The US5936103 patent is about me ... |
31-3-2007 at 05:48 by: Nicodem |
Pyridine hydrogenation - methods? [quote][i]Originally posted by MattEx[/i]
You said: [i]"Anyway, this is obviously irrelevant since ... |
31-3-2007 at 01:16 by: Nicodem |
Eschweiler-Clarke for Ethyl or Propyl groups [quote][i]Originally posted by Nicodem[/i]
The Leuckart reaction with aldehydes containing alpha-hy ... |
30-3-2007 at 01:49 by: Nicodem |
n-methyl-3,4-Dihydroxyphenylalanine (orgsyn) [quote][i]Originally posted by tupence_hapeny[/i]
So, back to the title reaction, the double-bond c ... |
30-3-2007 at 01:12 by: Nicodem |
n-methyl-3,4-Dihydroxyphenylalanine (orgsyn) I can work with concentrated aqueous HI any time I want without worrying about any legal consequence ... |
29-3-2007 at 03:45 by: Nicodem |
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