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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1868424생성일: 2026년 10월 25일

Benzo(b)thiophene, 3-bromo- → N-(1-Benzo[b]thiophen-3-ylmethyl-2,2,2-trifluoroethyl)-2,4,6-trimethylbenzenesulfonamide

https://huagongshe.com/reaction/1868424

반응식

참여 물질

역할이름HCID투입량
반응물Benzo(b)thiophene, 3-bromo-HCID 123250—
반응물MagnesiumHCID 5462224—
반응물2-Trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridineHCID 57474036—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TetrahydrofuranHCID 8028—
생성물N-(1-Benzo[b]thiophen-3-ylmethyl-2,2,2-trifluoroethyl)-2,4,6-trimethylbenzenesulfonamideHCID 1157551423.4%

반응 조건

온도80 °C

반응 단계

A mixture of 9 mg (2.20 mmol) of magnesium powder, 79 mg (0.37 mmol) of 3-bromobenzo[b]thiophene, 8 mg (0.04 mmol) of copper (I) iodide, and 50 mg (0.17 mmol) of 2-trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridine in 1 mL of THF was warmed at 80° C. in a sealed tube. After 30 minutes, the reaction was quenched with 7 mL of saturated aqueous ammonium chloride solution and extracted with three 7 mL portions of ethyl acetate. The combined organic layers were washed with two 5 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude material was chromatographed on silica gel using dichloromethane-hexanes (1:1) to load the sample and then eluting with dichloromethane-hexanes (1:1, then 75:25). The material from the column was triturated with ether-hexanes to afford 17 mg (23%) of the title compound as a white solid which is consistent with the desired product. MS: m/z 428.51 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07635711B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-ca8804da21c84c98af4f2a782c9c84b0
출처 메모uspto-grants-2009_12