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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

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물DiisopropylethylamineHCID 81531—
반응물tert-Butyl 4-bromobutanoateHCID 2757253—
반응물Benzoic acid, 3-mercapto-5-(trifluoromethyl)-, methyl esterHCID 68203827—
용매AcetonitrileHCID 6342—
생성물3-(3-tert-Butoxycarbonyl-propylsulfanyl)-5-trifluoromethyl-benzoic acid methyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748434B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-448051f2358b4aeab4e59db3d63c93fb
출처 메모uspto-grants-2014_06