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3,4-methylenedioxybenzoic acid to 3,4-methylenedioxybenzene?
Hi. I wonder if there's anything on this. Maybe a decarboxylation would work. Any articles? Thoughts ... |
14-1-2013 at 12:31
by: ChemistryGhost |
Extraction of caffeine with diethyl ether
What about caffeine extraction using 2-methyl-2-butanol. |
4-11-2012 at 15:52
by: ChemistryGhost |
Water flouridation
Oh well, live and learn. I can't speak of the mind control agents that actually work. It's pretty di ... |
28-10-2012 at 13:45
by: ChemistryGhost |
Water flouridation
Fluoride occurs naturally in sea water at less than 1 part per million, but it's balanced by 1 part ... |
28-10-2012 at 12:34
by: ChemistryGhost |
1-chloro-3,4-methylenedioxybenzene to 3,4-methylenedioxy-phenylacetaldehyde
Can 1-chloro-3,4-methylenedioxybenzene react with acetaldehyde in an enolate substitution reaction t ... |
26-10-2012 at 17:45
by: ChemistryGhost |
Ethylamine Synthesis
Ammonium chloride condenses with formaldehyde to form methyleneimine. Can a grignard reaction be don ... |
26-10-2012 at 14:59
by: ChemistryGhost |
Science Madness Forum BLOCKED (?) Part 2
It was down for just a few days. It was just a downed server and it was being updated. I'm noticing ... |
22-10-2012 at 14:50
by: ChemistryGhost |
Will it dissolve?
Cl2 reaction with chloride is ethylchloride(chloroethane). Does it just happen without the grignard ... |
13-10-2012 at 10:33
by: ChemistryGhost |
Will it dissolve?
I think 1,1-difluoroethane is nonpolar and chlorine is nonpolar as well. Will chlorine gas dissolve ... |
11-10-2012 at 17:13
by: ChemistryGhost |
Nucleophilic Substitution
I was thinking would it be possible to do an enolate subtitution(nucleophilic substitution) of ethan ... |
10-10-2012 at 14:23
by: ChemistryGhost |
Facing eviction because of experiment 20 months ago.
It's all fear and a mild brainwashing to make people comply to what big brother says. They want a fe ... |
4-10-2012 at 14:58
by: ChemistryGhost |
Ethylamine Synthesis
Maybe ethylamine can be obtained via ethanol and a tosyl chloride intermediate. Then reacting the in ... |
4-10-2012 at 13:22
by: ChemistryGhost |
Nitrostyrene-like reduction
Now's my chance before this possibly gets sent to detritus!
It's pronounced Cule (like in cube). No ... |
4-10-2012 at 13:03
by: ChemistryGhost |
Will the ester survive?
Reacting the chloride portion with the OH part of something like 1-Naphthol. 
[file]20297[ ... |
24-9-2012 at 12:17
by: ChemistryGhost |
Will the ester survive?
If someone tried to make an ester out of this and condense the chloride portion of 4-chloro-3-hydrox ... |
22-9-2012 at 15:18
by: ChemistryGhost |
Science Madness Forum BLOCKED (?) Part 2
For the last few days, Science Madness seemed to be blocked. Whenever I looked it up and clicked it, ... |
20-9-2012 at 12:32
by: ChemistryGhost |
R-Hydroxylamine decomposition to R-Ammonia?
Can R-hydroxylamine be reduced to R-amine by heating it? Possibly to between 100 to 120 degrees cels ... |
16-9-2012 at 15:28
by: ChemistryGhost |
Enols and Enamines?
I found this.
http://www.sciencemag.org/content/337/6099/1203.abstract
So can vinyl alcohol be pro ... |
16-9-2012 at 13:29
by: ChemistryGhost |
Enols and Enamines?
For the second one, i found out the product is called Vinyl alcohol. It's unstable and readily conve ... |
16-9-2012 at 13:10
by: ChemistryGhost |
Enols and Enamines?
[rquote=259710&tid=21479&author=zed]Sulfuric acid is not required. Acetone and Ethylamine s ... |
15-9-2012 at 15:04
by: ChemistryGhost |
Enols and Enamines?
So in the first one, does it only work with secondary amines? |
14-9-2012 at 11:32
by: ChemistryGhost |
Enols and Enamines?
Can it be possible to create (I don't know what it's called, let's call it ethylamine acetonate for ... |
13-9-2012 at 14:33
by: ChemistryGhost |
Ethylamine Synthesis
What about ethylamine dissolved in acetonitrile and using an amalgamation type reaction with Al/Mg ( ... |
13-9-2012 at 14:10
by: ChemistryGhost |
Ethylamine Synthesis
[rquote=259258&tid=18598&author=zed]Jeeze, buy some Platinum, produce some catalyst, and hyd ... |
13-9-2012 at 14:08
by: ChemistryGhost |
Isopropyl acetate to Isopropanol and acetic acid?
Is there a way to convert Isopropyl acetate to Isopropanol and acetic acid? |
10-9-2012 at 01:48
by: ChemistryGhost |
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