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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15229생성일: 2026년 10월 26일

Ammonium Chloride → 1-Tert-butoxycarbonyl-4-[2-(4-chloro-phenylsulfanyl)-5-trifluoromethyl-phenyl]-piperidine-4-ol

https://huagongshe.com/reaction/15229

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물1-Bromo-2-(4-chlorophenylsulfanyl)-5-(trifluoromethyl)benzeneHCID 68683413—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Tert-butoxycarbonyl-4-[2-(4-chloro-phenylsulfanyl)-5-trifluoromethyl-phenyl]-piperidine-4-olHCID 68684690—

반응 단계

A solution of n-butyl lithium (2.5 M in hexane, 6.5 mL, 16.2 mmol) was slowly added to a stirred solution of 1-bromo-2-(4-chlorophenylsulfanyl)-5-(trifluoromethyl)benzene (5.96 g, 16.2 mmol) in dry THF (40 mL) under argon at −78° C. The solution was stirred for 10 min before 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (3.23 g, 16.2 mmol) was added in one portion. The solution was allowed to warm to rt and then stirred overnight. Saturated aqueous ammonium chloride (80 mL) was added and the solution was extracted with ethyl acetate (80 mL). The organic phase was washed with saturated aqueous sodium chloride (50 mL), dried over magnesium sulfate and the solvent was evaporated off. The crude product was purified by flash chromatography on silica gel (eluent: ethyl acetate/heptane 2:8) to produce the target compound as a white foam, yield: 4.53 g (57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732463B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e0a36d7253684b78aae29694191ea28d
출처 메모uspto-grants-2010_06