From: Merlin (medchem$##$att.net)
Date: Tue Nov 05 2002 - 21:48:32 EST
Dear colleagues:
Currently I am using BBr3 for demethylation of a aryl methyl ether to a
phenol.
My questions is: what are some ideas on deactivating the excess BBr3/HBr in
the reaction mixture?
This is to ensure that no remaining HBr can brominate the aromatic ring
system.
I have used MeOH followed by sat. NaHCO3 to reach a pH of 7-9; unfortunately
this yielded a very messy emulsion.
Thank you in advance.
Cheers!
-- George D. 'Merlin' McCallion Associate Research Scientist Chemical Development Sanofi-Synthelabo Research 25 Great Valley Parkway Malvern, PA 19355 United StatesOffice: 610.889.6294 Fax: 610.889.6367 E: George.McCallion$##$sanofi-synthelabo.com
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