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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456550생성일: 2026년 10월 25일

Acetyl chloride → 3-(1-Acetyl-piperidin-4-yl)-7-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/456550

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물3-Piperidin-4-yl-7-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid methyl esterHCID 58817652—
용매Ethyl AcetateHCID 8857—
생성물3-(1-Acetyl-piperidin-4-yl)-7-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid methyl esterHCID 5881757488%

반응 단계

To a room temperature solution of 3-piperidin-4-yl-7-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid methyl ester (4.37 g, 12.7 mmol), triethylamine (2.70 mL. 19.4 mmol), and anhydrous THF (80 mL) under nitrogen was added acetyl chloride (1.10 mL, 15.5 mmol) in one portion and the reaction stirred at room temperature overnight. The reaction was diluted with ethyl acetate (300 mL) and washed with water (150 mL) and brine (150 mL) successively. The organic layer was dried over magnesium sulfate, filtered, and the solvent removed. The residue was chromatographed on silica, eluting with 10% methanol/ethyl acetate, to afford 4.28 g (88%) of the desired product as a white solid, mp: 155.2° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186724B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-241fed9fba63418593d43959e35eb3cd
출처 메모uspto-grants-2007_03