REACTION OF PERFLUORO-4-METHYLPENTENE-2 WITH SECONDARY AMINES

doi:10.1246/CL.1972.577

Paper

REACTION OF PERFLUORO-4-METHYLPENTENE-2 WITH SECONDARY AMINES

Published 1972 · Goro Tsukamoto, Nobuo Ishikawa

Chemistry Letters

6

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0

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Abstract

Perfluoro-4-methylpentene-2 [1] , an asymmetrical internal perfluoroolefin, reacted with secondary amines such as diethylamine or piperidine to give a terminal enamine [2], which was easily hydrolyzed to the corresponding amide [3]. The reaction mechanism was discussed.

Study Snapshot

Perfluoro-4-methylpentene-2 reacts with secondary amines to produce a terminal enamine, which can easily be hydrolyzed to the corresponding amide.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

REACTION OF PERFLUORO-4-METHYLPENTENE-2 WITH SECONDARY AMINES

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