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HRID 403390作成日:2026年10月26日

Ethyl Acetate → 3-(3-tert-Butoxycarbonyl-propylsulfanyl)-5-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/403390

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物DiisopropylethylamineHCID 81531—
反応物tert-Butyl 4-bromobutanoateHCID 2757253—
反応物Benzoic acid, 3-mercapto-5-(trifluoromethyl)-, methyl esterHCID 68203827—
溶媒AcetonitrileHCID 6342—
生成物3-(3-tert-Butoxycarbonyl-propylsulfanyl)-5-trifluoromethyl-benzoic acid methyl esterHCID 68203828—

反応手順

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+]).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748434B2
出典データセットuspto-grants-2014_06
ORD IDord-448051f2358b4aeab4e59db3d63c93fb
出典メモuspto-grants-2014_06