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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683749Generated: October 27, 2026

Acrylonitrile → 3-[(3-Bromophenyl)thio]propionitrile

https://huagongshe.com/reaction/1683749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
Reactantm-BromobenzenethiolHCID 80597—
SolventSodium HydroxideHCID 14798—
Product3-[(3-Bromophenyl)thio]propionitrileHCID 1868674293.7%

Reaction Steps

3-Bromothiophenol (10 g, 52.9 mmmol) was dissolved in acrylonitrile (11.28 g, 213 mmol). Triton B (1 mL) was added, at which time the reaction mixture became exothermic and began to reflux without added heat. The mixture was allowed to cool to room temperature, poured into cold aqueous sodium hydroxide (2%; 200 mL), and extracted with diethyl ether. The organic layer was dried, filtered and evaporated to provide 12 g (93%) of 3-[(3-bromophenyl)thio]propionitrile as a tan oil; 1H NMR (CDCl3) δ 7.54 (s, 1H), 7.42 (d, 1H), 7.32 (d, 1H), 7.25-7.15 (m, 2H), 3.15 (t, 2H), 2.62 (t, 2H); Mass spectrum m/z 261, 259 (M+NH4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639759
Source datasetuspto-grants-1997_06
ORD IDord-8a606e206ad24afe8308f7c420b5f4ee
Source noteuspto-grants-1997_06