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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683311Generated: October 25, 2026

Acrylonitrile → N-(2-cyanoethyl)-N',N'-dimethyl-1,4-diaminobutane

https://huagongshe.com/reaction/1683311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
Reactant4-DimethylaminobutylamineHCID 77063—
SolventMethanolHCID 887—
ProductN-(2-cyanoethyl)-N',N'-dimethyl-1,4-diaminobutaneHCID 1893468080%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of acrylonitrile (1.17 g, 22.07 mmol) in methanol (1.0 ml) was added dropwise to a solution of N,N-dimethyl-1,4-diaminobutane 322 (2.1 g, 18.42 mmol) in methanol (10 ml) at 0° C. and the mixture was stirred at 0° C. for sixteen hours. Evaporation of the solvent in vacuo afforded almost pure N-(2-cyanoethyl)-N',N'-dimethyl-1,4-diaminobutane 323 as a colorless oil (2.5 g, 80% yield based on 322). 1H NMR (400 MHz, CDCl3) δ: 1.45 (4H, m, --CH2 --CH2 --CH2 --CH2 --), 2.15 (6H, s, --N(CH3)2), 2.22 (2H, t, --CH2N), 2.47 (2H, t, --CH2CH2CN), 2.60 (2H, t, --CH2CH2NH--), 2.88 (2H, t, --CH2CH2NH--), 3.37 (1H, s, --NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637691
Source datasetuspto-grants-1997_06
ORD IDord-d7a44922ea354b978d207aa551fd8187
Source noteuspto-grants-1997_06