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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1580463생성일: 2026년 10월 27일

Benzenesulfonamide → 1,1-Diphenylurea

https://huagongshe.com/reaction/1580463

반응식

참여 물질

역할이름HCID투입량
반응물BenzenesulfonamideHCID 7370—
반응물N,N-Diphenylcarbamic chlorideHCID 65741—
반응물SodiumHCID 5360545—
용매TolueneHCID 1140—
생성물1,1-DiphenylureaHCID 33603—

반응 단계

6.5 g of sodium salt of 4-(β-<2-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonamide were refluxed for 3 hours with 3.9 g of diphenylcarbamic acid chloride in 60 ml of toluene. The crude N-[4-(β-<2-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonyl]-N',N'-diphenyl-urea obtained was suction-filtered, suspended in dioxane and, after addition of 1 g of acetic acid and 1.6 g of cyclopentyl-amine, the substance was refluxed for 11/2 hours. After acidification with dilute hydrochloric acid the precipitate was separated by suction-filtration and treated with 0.5 %-ammonia. The aqueous alkaline solution was acidified and the crystals were re-crystallized from methanol. N-[4-(β-<2-methoxy-5-chloro-benzamido>-ethyl)-benzenesulfonyl] -N'-cyclopentyl-urea was obtained having a melting point of 182° - 184°C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03932658
출처 데이터셋uspto-grants-1976_01
ORD IDord-c2b243f10a594e45a5ba002fae0bdf1c
출처 메모uspto-grants-1976_01