Nucleophilic substitution of the acetoxy group in 3-methylbenzoylaminomethyl acetate

Replacement of the acetoxy group in 3-methylbenzoylaminomethyl acetate with N- and S-nucleophiles generated from amines and thio compounds using sodium hydride gives the corresponding N -aminomethyl- and N -thiomethylbenzamides.

Bibliographic Details

Published in:	Russian chemical bulletin Vol. 60; no. 8; pp. 1672 - 1676
Main Authors:	Labanauskas, L., Mazeikaite, R., Striela, R., Gedrimaite, O., Urbelis, G., Zilinskas, A.
Format:	Journal Article
Language:	English
Published:	Boston Springer US 01-08-2011
Subjects:	Chemistry Chemistry and Materials Science Chemistry/Food Science Full Articles Inorganic Chemistry Organic Chemistry aminals sodium hydride nucleophilic substitution of acetoxy group aminomethylbenzamides thiomethylbenzamides thioaminals sulfides
Online Access:	Get full text
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