Monomeric products from the condensation of phenol with formaldehyde and primary amines

WJ Burke, CW Stephens

Index: Burke; Stephens Journal of the American Chemical Society, 1952 , vol. 74, p. 1518

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Citation Number: 70

Abstract

Phenols having unsubstituted ortho or para positions have been shown to form Mannich bases by condensation with formaldehyde and either primar~~-~ or sec~ ndary~-~ amines. Reaction of phenol with formaldehyde and dimethylamine has been reported to give 2-7* 8 2, 6-bk7 and 2, 4, 6-tris-(dimethylaminomethyl)-phenol. 2, 4, 6-Tris-(morpholinomethy1)- phenol also has been prepared. s In the limited work with primary amines only resinous ...