Re: ORGLIST: Chlorination of primary amino alcohols

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From: Jeremy M. Carr (carr030$##$bama.ua.edu)
Date: Thu Oct 25 2007 - 12:12:47 EDT


Coupling might be problematic if you're using chlorides; this concept
isn't really stressed until upper level organic chemistry courses.
Have you tried brominating the ring instead with HOAc/Br2? Your
bromide should probably crash out at the end; wash it with water on
filtration and the acetic acid smell should eventually go away.

Good luck

-JMC
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