戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 54748作成日:2026年10月26日

o-Chlorophenylacetic acid → Acetyl chloride, 2-(2-chlorophenyl)-

https://huagongshe.com/reaction/54748

反応式

関与物質

役割名称HCID仕込み量
反応物o-Chlorophenylacetic acidHCID 17124—
反応物Thionyl ChlorideHCID 24386—
生成物Acetyl chloride, 2-(2-chlorophenyl)-HCID 182669—

反応手順

15 ml of thionyl chloride was added to 0.44 g of 2-chlorophenylacetic acid. The mixture was stirred at room temperature for 2 hours. The reaction mixture was subjected to distillation to remove the remaining thionyl chloride and then to azeotropy with toluene twice to completely remove the thionyl chloride. The residue was dissolved in 10 ml of dichloromethane. 0.36 ml of triethylamine was added, with ice-cooling, to a dichloromethane solution containing 0.40 g of 5-dimethylamino-1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzoazepine. Thereto was dropwise added the above obtained 2-(2-chlorophenyl)acetyl chloride solution. The resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was water-washed twice, then dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (elutant: chloroform/methanol=200/1) and then recrystallized from methanol-diethyl ether to obtain 0.29 g of 5-dimethylamino-1-{4-[2-(2-chlorophenyl)acetylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzoazepine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622947
出典データセットuspto-grants-1997_04
ORD IDord-d0c460ed1540444c85bf2a050d61eee3
出典メモuspto-grants-1997_04