The Vespiary
The Hive => Chemistry Discourse => Topic started by: Vibrating_Lights on August 10, 2004, 03:15:00 AM
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Could 1,4 chlorobutane be hydrolized in the same manners as the standard BzCl-BzOH methods to give 1,4 butandiol
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That is unlikely, as the intermediate 4-chlorobutanol will cyclize to tetrahydrofuran under basic conditions.
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Can NaOH in MeOH not be used to hydrolize Gaba for Na:GHB.
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There is nothing in the GABA molecule that can be hydrolized. You need to transform the amino group into a hydroxy in order to get GHB. There are numerous threads dealing with this reaction (nitrosation of GABA).
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If it gets converted to tetrahydrofuran (THF) in the body, then you'll definately get a GHB-like buzz. I've ingested 4ml THF at a time without any shitty side-effects; just sweet euphoria, but I've done this several times, and I don't know how my liver is doing. Is there some sort of test that my Dr. can give me or am I up shit creek without a paddle? I don't know if my liver is slop. Any suggestions?
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Bwiti:
Possibly the standart test will do the work:
Aspartate aminotransferase (AST or SGOT) - must be <40
Alanine aminotransferase (ALT or SGTP) - must be <40
Gamma-glutamyl transpeptidase (GGTP, GGT) - must be <60
But if your values are a little bit higher do not worry, just stop for about 1-2 months your biological experiments.
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you can use a base to alkylate acetophenone with that 1,4 dichlorobutane and skip right to the middle of the ketamine synthesis. You can make pyrrolle with it also. I'd probably save the stuff for some cool experiments.