돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47815생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/47815

반응식

참여 물질

역할이름HCID투입량
반응물1-HeptanamineHCID 8127—
반응물Thionyl ChlorideHCID 24386—
반응물Benzeneacetic acid, 4-bromo-HCID 74654—
반응물DiisopropylethylamineHCID 81531—
용매WaterHCID 962—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물2-(4-bromo-phenyl)-N-heptyl-acetamideHCID 4475836—

반응 단계

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%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699904B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-25fe1573b1714939984f8e042e7152fd
출처 메모uspto-grants-2004_03