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HRID 22268作成日:2026年10月25日

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

https://huagongshe.com/reaction/22268

反応式

関与物質

役割名称HCID仕込み量
反応物AcrylonitrileHCID 7855—
反応物m-BromobenzenethiolHCID 80597—
溶媒Sodium HydroxideHCID 14798—
生成物3-[(3-Bromophenyl)thio]propionitrileHCID 1868674293.7%

反応手順

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) δ7.54 (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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428040
出典データセットuspto-grants-1995_06
ORD IDord-e11ad11d2499429e80643360e0a1b5f0
出典メモuspto-grants-1995_06