戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 486084作成日:2026年10月26日

Carbon tetrabromide → N-(5-bromopentyl)-N'-(2,4-difluorophenyl)-N-heptylurea

https://huagongshe.com/reaction/486084

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon tetrabromideHCID 11205—
反応物TriphenylphosphineHCID 11776—
反応物Urea, N'-(2,4-difluorophenyl)-N-heptyl-N-(5-hydroxypentyl)-HCID 11725825—
溶媒DichloromethaneHCID 6344—
生成物N-(5-bromopentyl)-N'-(2,4-difluorophenyl)-N-heptylureaHCID 10342005100%

反応手順

Part D. To a solution of N'-(2,4-difluorophenyl)-N-heptyl-N-5-hydroxypentylurea (15.0 g, 0.042 mol) and carbon tetrabromide (16.75 g, 0.051 mol) in methylene chloride (350 mL) under a nitrogen atmosphere at ambient temperature, a solution of triphenylphosphine (13.24 g, 0.051 mol) in methylene chloride (100 mL) was added slowly. The reaction mixture was stirred for 3 hours and was concentrated in vacuo to give crude viscous oil. The product was purified by flash chromatography on silica gel (400 mL) eluting with hexane:ethyl acetate (90:10::v:v) to give N-(5-bromopentyl)-N'-(2,4-difluorophenyl)-N-heptylurea as a viscous colorless oil (17.5 g, 0.042 mol). 1H NMR (CDCl3) δ8.14-8.00 (m,1H), 6.92-6.79 (m,2H), 6.35 (bs,1H), 3.49-3.25 (m,6H), 1.99-1.26 (m,16H), 0.92 (t,3H,J=6.7 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05290801
出典データセットuspto-grants-1994_03
ORD IDord-18efbdd258a649289ce167f1fd9aaf0a
出典メモuspto-grants-1994_03