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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38225생성일: 2026년 10월 25일

Methanesulfonyl chloride → N-(3-ethynylphenyl)methanesulfonamide

https://huagongshe.com/reaction/38225

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물Benzenamine, 3-ethynyl-HCID 104682—
용매PyridineHCID 1049—
생성물N-(3-ethynylphenyl)methanesulfonamideHCID 57131399—

반응 단계

To a solution of 3-ethynyl aniline (1.05 mL, 10.0 mmol) in pyridine (5 mL) was added methanesulfonyl chloride (857 μL, 1.10 eq.) at a temperature of 0° C. The resulting mixture was stirred overnight at room temperature and was then evaporated. The residue was treated with 2 N aq. HCl (25 mL) and subsequently extracted with ethyl acetate (2×30 mL). The combined organic layers were dried over MgSO4 and evaporated to give the desired methanesulfonamide in quantitative yield. It was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524724B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-e04eb91ca7634a4a97f9b40e63bc61d3
출처 메모uspto-grants-2013_09