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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481986생성일: 2026년 10월 24일

Triethylamine → Benzenesulfonamide

https://huagongshe.com/ko/reaction/481986

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물N,N-Bis(2-hydroxyethyl)-4-methylbenzenesulfonamideHCID 81565—
용매DichloromethaneHCID 6344—
생성물BenzenesulfonamideHCID 737085.7%

반응 단계

A solution of 11.4 g (0.1 mole) of methanesulfonyl chloride in 17.1 ml of dichloromethane is cooled to 5° C. A solution of 13 g (0.05 mole) of N,N-bis(2-hydroxyethyl)-4-methylbenzenesulfonamide and 10.1 g (0.1 mole) of triethylamine in 52 ml of dichloromethane is then added dropwise with stirring. The resulting mixture is allowed to return to ambient temperature and stirred for a further 3 hours. The reaction mixture is then extracted three times with 40 ml water. The organic phase is dried over sodium sulfate, filtered and concentrated in a rotating evaporator. The resulting oil is then crystallized from ethanol. 17.8 g of 4-methyl-N,N-bis[2-methylsulfonyloxy)ethyl]benzenesulfonamide are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05792770
출처 데이터셋uspto-grants-1998_08
ORD IDord-ccc72a90f7184e26b8ea2436581a081a
출처 메모uspto-grants-1998_08