戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 47815作成日:2026年10月26日

1-Heptanamine → 2-(4-bromo-phenyl)-N-heptyl-acetamide

https://huagongshe.com/reaction/47815

反応式

関与物質

役割名称HCID仕込み量
反応物1-HeptanamineHCID 8127—
反応物Thionyl ChlorideHCID 24386—
反応物Benzeneacetic acid, 4-bromo-HCID 74654—
反応物DiisopropylethylamineHCID 81531—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物2-(4-bromo-phenyl)-N-heptyl-acetamideHCID 4475836—

反応手順

A stirred solution of (4-bromo-phenyl)-acetic acid (0.186 mol, 40.0 g) and thionyl chloride (0.558 mol, 40.0 mL) in chloroform (500 mL) under a N2 atmosphere was heated under reflux for 20 hours. The mixture was cooled to room temperature and evaporated under vacuum to give an oil. This was dissolved in anhydrous methylene chloride (150 mL) and added dropwise to a solution of heptylamine (0.20 mol, 30.3 mL) and N,N-diisopropylethylamine (0.37 mol, 64.7 mL) in anhydrous methylene chloride cooled to 0° C. The mixture was stirred at room temperature for 45 minutes then poured into water and extracted with methylene chloride. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and the solvent was removed under vacuum. The solid residue was purified by crystallization from ethyl acetate/hexanes to give 2-(4-bromo-phenyl)-N-heptyl-acetamide as a white solid. (37 g, 64%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699904B2
出典データセットuspto-grants-2004_03
ORD IDord-25fe1573b1714939984f8e042e7152fd
出典メモuspto-grants-2004_03