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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1395724생성일: 2026년 10월 26일

Methanesulfonamide → N-{4-[15-(Trifluoromethyl)pentadecylamino]-benzoyl}methanesulfonamide

https://huagongshe.com/reaction/1395724

반응식

참여 물질

역할이름HCID투입량
반응물MethanesulfonamideHCID 72879—
반응물4-[15-(Trifluoromethyl)pentadecylamino]benzoyl chloride hydrochlorideHCID 20549317—
용매PyridineHCID 1049—
생성물N-{4-[15-(Trifluoromethyl)pentadecylamino]-benzoyl}methanesulfonamideHCID 20549394—

반응 단계

A solution of 25.2 g. of 4-[15-(trifluoromethyl)pentadecylamino]benzoyl chloride hydrochloride and 5.6 g. of methanesulfonamide in 250 ml. of pyridine is stirred under reflux for 2 hours and then concentrated in vacuo. The residue is partitioned between water and diethyl ether; the aqueous layer acidified with 1 N hydrochloric acid, and the organic layer separated, dried over magnesium sulfate and evaporated. Crystallization of the residual white solid from 60% aqueous acetic acid and then from methylene chloride-hexane affords the product as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04205085
출처 데이터셋uspto-grants-1980_05
ORD IDord-910e4743b6844a52b72e48e03ad06c9a
출처 메모uspto-grants-1980_05