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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzo(b)thiophene, 3-bromo- | HCID 123250 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | 2-Trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridine | HCID 57474036 | — |
| 촉매 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(1-Benzo[b]thiophen-3-ylmethyl-2,2,2-trifluoroethyl)-2,4,6-trimethylbenzenesulfonamide | HCID 11575514 | 23.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07635711B2 |
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| 출처 데이터셋 | uspto-grants-2009_12 |
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| ORD ID | ord-ca8804da21c84c98af4f2a782c9c84b0 |
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| 출처 메모 | uspto-grants-2009_12 |
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