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OfflineChemiker
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Male
Registered: 12/05/06
Posts: 367
Last seen: 17 years, 2 months
Re: GHB chemistry question. [Re: Shmoppy McGillicuddy]
    #6395026 - 12/21/06 07:38 PM (17 years, 3 months ago)

Cleavage to produce a benzyl species would not be useful. It would, at most split the molecule into three framents, essentially:
(1) toluene (3) methylamine and (3) acetic acid. This would be of very little use and would require a lot of energy to pull off because it involves cleavage of two covalent bonds.

You may object that there are other possible ways to acheive benzylic cleavage, but only this type of cleavage would be of synthetic use for you. Any other way would still face the problem of losing the phenyl group.

Remember, benzylic = Ph-CH3 , not just Ph.

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OfflineSchwip
Never sleeps.
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Registered: 06/27/05
Posts: 3,937
Last seen: 11 years, 4 months
Re: GHB chemistry question. [Re: Schwip]
    #6634405 - 03/04/07 01:39 PM (17 years, 29 days ago)

So....curious if anyone has put anymore thoughts into this?

Anyone give this a go yet(where legal)?


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