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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1868419생성일: 2026년 10월 26일

4-Toluenesulfonyl chloride → 2-Trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridine

https://huagongshe.com/reaction/1868419

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Sodium hydrideHCID 24758—
반응물2,4,6-trimethyl-N-(2,2,2-trifluoro-1-hydroxymethylethyl)benzenesulfonamideHCID 57474035—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-Trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridineHCID 5747403699.8%

반응 단계

To a solution of 690 mg (2.22 mmol) of 2,4,6-trimethyl-N-(2,2,2-trifluoro-1-hydroxymethylethyl)benzenesulfonamide in 10 mL of THF was added 180 mg (4.5 mmol) of 60% sodium hydride in mineral oil in several portions followed by 475 mg (2.5 mmol) of p-toluenesulfonyl chloride. The mixture stirred at room temperature over night and was then diluted with water and extracted with three 20 mL portions of ethyl acetate. The combined organic layers were washed with three 20 mL portions of saturated aqueous sodium bicarbonate solution, 20 mL of brine, and two 20 mL portions of saturated aqueous ammonium chloride solution, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 650 mg (99%) of 2-trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridine as an oil which solidified to a waxy solid upon standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07635711B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-79aac52b5d7a482597ed54706951fe29
출처 메모uspto-grants-2009_12