Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 403390생성일: 2026년 10월 25일
Ethyl Acetate → 3-(3-tert-Butoxycarbonyl-propylsulfanyl)-5-trifluoromethyl-benzoic acid methyl ester
https://huagongshe.com/reaction/403390
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | tert-Butyl 4-bromobutanoate | HCID 2757253 | — |
| 반응물 | Benzoic acid, 3-mercapto-5-(trifluoromethyl)-, methyl ester | HCID 68203827 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 3-(3-tert-Butoxycarbonyl-propylsulfanyl)-5-trifluoromethyl-benzoic acid methyl ester | HCID 68203828 | — |
반응 단계
To a solution of 3-mercapto-5-trifluoromethyl-benzoic acid methyl ester (990 mg, 4.19 mmol) in acetonitrile (25 mL) were added N,N-diisopropylethylamine (1.08 g, 1.46 mL, 8.38 mmol) and tert-butyl 4-bromobutanoate (935 mg, 4.19 mmol, CAS RN 110611-91-1). The clear yellow solution was stirred at room temperature for 2.5 hours and then poured on water and ethyl acetate and the layers were separated. The aqueous layer was extracted twice with ethyl acetate. The organic layers were washed with brine, dried over magnesium sulfate, filtered, treated with silica gel and evaporated. The compound was purified by silica gel chromatography on a 50 g column using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:ethyl acetate (100:0 to 70:30). Light yellow liquid (1.27 g, 80%). MS (ESI+): m/z=379 ([M+]).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08748434B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-448051f2358b4aeab4e59db3d63c93fb |
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| 출처 메모 | uspto-grants-2014_06 |
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