Author:
Fujiwara Allan N.,Acton Edward M.
Abstract
Nitration of 2,5-dimethylbenzoic acid was only 29% at the meta2 position vs. 41% at the ortho, in contrast to sulfonation which was 85% meta vs. 15% para. Identity of the products (and of their derived amino esters and phenolic esters) was determined from the nuclear magnetic resonance spectra and confirmed by chemical means.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
2 articles.
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