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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58857생성일: 2026년 10월 24일

2-Aminobenzyl alcohol → N-(2-(hydroxymethyl)phenyl)methanesulfonamide

https://huagongshe.com/ko/reaction/58857

반응식

참여 물질

역할이름HCID투입량
반응물2-Aminobenzyl alcoholHCID 21439—
반응물Methanesulfonyl chlorideHCID 31297—
용매PyridineHCID 1049—
용매ChloroformHCID 6212—
생성물N-(2-(hydroxymethyl)phenyl)methanesulfonamideHCID 2295581553.8%

반응 단계

A solution of methane sulfonyl chloride (10.2 ml, 0.13 mol) in chloroform (100 mL) was added dropwise to a solution of (2-aminophenyl)methanol (15.0 g, 0.12 mol) in pyridine (100 mL) and chloroform (150 mL) under nitrogen over 1 h at 0° C. The reaction mixture was stirred for 12 h at ambient temperature and then washed with hydrochloric acid (2N, 200 ml×2). The organic phase was dried over anhydrous MgSO4 and concentrated. The residue was purified by flash column chromatography on silica gel (EtOAc/hexane=1:3) to afford N-[2-(hydroxymethyl)phenyl]methanesulfonamide (13.0 g, 53% yield) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434761B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-cc7c2c09648b42f9ab0908c369380260
출처 메모uspto-grants-2016_09