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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261203Generated: October 26, 2026

Propanenitrile, 3-(methylamino)- → 3-[N-(p-chlorocinnamyl)-methylamino]propionitrile

https://huagongshe.com/reaction/261203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanenitrile, 3-(methylamino)-HCID 69656—
Reactantp-Chlorocinnamyl bromideHCID 53877224—
CatalystBenzenemethanaminium, N,N,N-tributyl-, bromideHCID 2724282—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product3-[N-(p-chlorocinnamyl)-methylamino]propionitrileHCID 54351008—

Reaction Steps

A solution of 116 g of p-chlorocinnamyl bromide in 500 ml of methylene chloride is added dropwise with stirring to a mixture of 42 g of 3-methylamino-propionitrile and 8.9 g of benzyl-tri-(n-butyl)ammonium bromide in 1 liter of methylene chloride and 500 ml of 2 N sodium hydroxide solution at room temperature and under a nitrogen atmosphere, and the emulsion stirred for 65 hours at room temperature. The organic phase is separated, washed with water, dried over sodium sulphate and evaporated to yield 3-[N-(p-chlorocinnamyl)-methylamino]-propionitrile. M.P. 143° [hydrogen oxalate form]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04164583
Source datasetuspto-grants-1979_08
ORD IDord-e42bef5d4dd8458b8cd112224d2d9d0c
Source noteuspto-grants-1979_08