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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194116Generated: October 25, 2026

3-(Dimethylamino)prop-2-enenitrile → 3-(2,3-Dichlorophenacylamino)acrylonitrile

https://huagongshe.com/reaction/1194116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Dimethylamino)prop-2-enenitrileHCID 97497—
ReactantEthanone, 2-amino-1-(2,3-dichlorophenyl)-, hydrochlorideHCID 22151845—
SolventEthanolHCID 702—
Product3-(2,3-Dichlorophenacylamino)acrylonitrileHCID 67944094—

Reaction Steps

20.0 g of 2,3-dichlorophenacylamine hydrochloride and 10.0 g of 3-dimethylaminoacrylonitrile are heated for 1 hour under reflux in 300 ml of ethanol. After cooling it to room temperature, the reaction solution is poured into a mixture of ice/dilute hydrochloric acid. After extraction with ethyl acetate, the combined extracts are dried over sodium sulfate, filtered, and the filtrate is concentrated. The oily residue is purified by column chromatography (silica gel: elution with a 4:1 mixture of toluene/ethyl acetate). M.p. 125°-127° C. IR (solid/KBr) in cm-1 : 3380 (NH), 2200 (CN), 1715 (CO) 1625 (C=C). 1H-NMR (DMSOd6) in ppm: 4.09 (d, J=15 Hz, 1H); 4.46 (d, J=7 Hz, 2H); 7.2 (q, 1H); 7.4 (broad s, 1H); 7.45-7.85 (m, 3H). Mass spectrum: molecular peak at 254.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04812580
Source datasetuspto-grants-1989_03
ORD IDord-c4e8cc3781ba4076ace4c232ff00600c
Source noteuspto-grants-1989_03