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HRID 129647作成日:2026年10月26日

Triethylamine → 2-(p-Chlorophenyl)-5-[(trifluoromethyl)thio]pyrrole-3-carbonitrile

https://huagongshe.com/reaction/129647

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-ChloroacrylonitrileHCID 70198—
反応物Trifluoromethyl 1-chloro-N-(p-chlorobenzyl)thioformimidateHCID 18930385—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物2-(p-Chlorophenyl)-5-[(trifluoromethyl)thio]pyrrole-3-carbonitrileHCID 1893039257.8%

反応手順

Under a nitrogen purge, a solution of trifluoromethyl-1-chloro-N-(p-chlorobenzyl)thioformimidate (1.1 g, 0.004 mol) and 2-chloroacrylonitrile (0.4 mL, 0.005 mol) is treated with a solution of triethylamine (1.3 mL, 0.009 mol) in toluene. After an induction period, solids begin to form as the reaction mixture exotherms slightly. When the exotherm subsides, the reaction mixture is heated at reflux temperature for 16 hours, cooled and filtered. The filter cake is washed with ethyl acetate and the filtrate is concentrated in vacuo to obtain a semi-solid. The semi-solid is dissolved in ethyl acetate and the organic solution is washed with water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a solid. The solid is twice recrystallized from 1,2-dichloroethane to give the title product as a beige solid (0.7 g, mp 203°-205° C.) which is identified by 1HNMR spectral analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05468877
出典データセットuspto-grants-1995_11
ORD IDord-a099147a108340039e6a16d88b514b47
出典メモuspto-grants-1995_11