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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486084생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/486084

반응식

참여 물질

역할이름HCID투입량
반응물Carbon tetrabromideHCID 11205—
반응물TriphenylphosphineHCID 11776—
반응물Urea, N'-(2,4-difluorophenyl)-N-heptyl-N-(5-hydroxypentyl)-HCID 11725825—
용매DichloromethaneHCID 6344—
생성물N-(5-bromopentyl)-N'-(2,4-difluorophenyl)-N-heptylureaHCID 10342005100%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05290801
출처 데이터셋uspto-grants-1994_03
ORD IDord-18efbdd258a649289ce167f1fd9aaf0a
출처 메모uspto-grants-1994_03