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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242562생성일: 2026년 10월 23일

tert-Butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate → 4-(4-Chloro-phenyl)-4-hydroxy-3,3-dimethyl-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/242562

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylateHCID 22278899—
반응물HCID 178478191HCID 178478191—
용매TetrahydrofuranHCID 8028—
생성물4-(4-Chloro-phenyl)-4-hydroxy-3,3-dimethyl-piperidine-1-carboxylic acid tert-butyl esterHCID 59341212—

반응 단계

To an ice-cooled solution 3,3-Dimethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester (1.6 g, 7.2 mmol) in THF (20 mL) was added 4-chlorophenylmagnesium bromide (1 M in ether, 15 mL, 15 mmol). The solution was allowed to warm to about room temperature, then stirred at room temperature for about 22 hours. The reaction was quenched with aqueous ammonium chloride and extracted with ethyl acetate. The combined organic layers were concentrated in vacuo, then purified by flash chromatography on silica gel (35 g SiO2, gradient elution from 100% hexane to 100% ethyl acetate) to yield the title compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653096B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-78bdd389d3534e50b6c0cd096fb8ef8e
출처 메모uspto-grants-2014_02