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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501324생성일: 2026년 10월 26일

Trifluoroacetic acid → 3-Piperidin-4-yl-7-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/501324

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Potassium CarbonateHCID 11430—
반응물4-(3-Hydroxy-2-methoxycarbonyl-7-trifluoromethyl-2,3-dihydro-benzo[b]thiophen-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 68455372—
용매DichloromethaneHCID 6344—
생성물3-Piperidin-4-yl-7-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid methyl esterHCID 58817652—

반응 조건

온도40 °C

반응 단계

To a room temperature solution of 4-(3-hydroxy-2-methoxycarbonyl-7-trifluoromethyl-2,3-dihydro-benzo[b]thiophen-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (6.00 g, 13.0 mmol) in DCM (30 mL) was added TFA (30 mL) causing rapid gas evolution. After 5 min, the reaction was stirred at 40° C. for 5.5 h. After cooling to room temperature, the reaction was poured into 20% aqueous potassium carbonate (400 mL) and extracted with DCM (2×200 mL). The combined extracts were dried over magnesium sulfate, filtered, and the solvent removed to give a thick oil. After drying under high vacuum 4.37 g (98%) of the desired product was obtained as a white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772252B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-29302c7e22f74c8a881b13da7a691f52
출처 메모uspto-grants-2010_08