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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456548생성일: 2026년 10월 25일

Tetrahydrofuran → 4-(3-Hydroxy-2-methoxycarbonyl-7-trifluoromethyl-2,3-dihydro-benzo[b]thiophen-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/456548

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Methyl ThioglycolateHCID 16907—
반응물Sodium hydrideHCID 24758—
반응물4-(2-Fluoro-3-trifluoromethyl-benzoyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 58817540—
용매Ethyl AcetateHCID 8857—
용매Ethylacetate heptaneHCID 21899848—
생성물4-(3-Hydroxy-2-methoxycarbonyl-7-trifluoromethyl-2,3-dihydro-benzo[b]thiophen-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 6845537256%

반응 조건

온도55 °C

반응 단계

To a room temperature solution of 4-(2-fluoro-3-trifluromethyl-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester (9.00 g, 24.0 mmol), methyl thioglycolate (2.40 mL, 26.8 mmol), and anhydrous THF (200 mL) under nitrogen was added NaH (1.15 g of a 60% oil dispersion, 28.7 mmol) in one portion. After the gas evolution ceased, the reaction was stirred at 55° C. After 100 min, the reaction was cooled to room temperature and diluted with ethyl acetate (500 mL). The mixture was washed with water (300 mL) and brine (300 mL) successively, dried over magnesium sulfate, filtered, and the solvent removed to afford a sticky white solid. Trituration with 20% ethyl acetate/heptane afforded 6.20 g (56%) of the desired product as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186724B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-9923cee5fca14061a9f582b31d5fde77
출처 메모uspto-grants-2007_03