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I was reading through my textbook and apparently when 4-aminophenol reacts with an acyl chlordie / acid anhydride (as in the synthesis of paracetamol) only the R-NH2 group reacts and NOT the R-OH group.Why is this?
It doesn't, not always. See http://books.google.co.uk/books?id=LXJ_62eaejoC&pg=PP36&lpg=PP36&dq=chemoselectivity+in+aminophenols&source=bl&ots=F3-sPTxWcl&sig=d7yihneo6G1TIZ5170XNj624Xx4&hl=en&sa=X&ei=KGm1T-zsA-XS0QWes5zlAw&ved=0CFEQ6AEwAA#v=onepage&q=chemoselectivity%20in%20aminophenols&f=false
The first page of this link shows you reaction of p-aminophenol with TsCl.
Quote from: AWK on May 18, 2012, 03:11:23 AMThe first page of this link shows you reaction of p-aminophenol with TsCl.my question was SPECIFIC to the reaction of acid anhydride / acid chloride (R-COCl) which TsCl is not...
Because the nitrogen is more nucleophillic than the oxygen atom?
Quote from: discodermolide on May 18, 2012, 05:22:42 AMBecause the nitrogen is more nucleophillic than the oxygen atom?in excess would the -OH group also react?
Quote from: AWK on May 18, 2012, 03:11:23 AMThe first page of this link shows you reaction of p-aminophenol with TsCl.TsCl is an acid chloride!
acid chloride (R-COCl)