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HRID 242562作成日:2026年10月24日

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/ja/reaction/242562

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylateHCID 22278899—
反応物HCID 178478191HCID 178478191—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Chloro-phenyl)-4-hydroxy-3,3-dimethyl-piperidine-1-carboxylic acid tert-butyl esterHCID 59341212—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653096B2
出典データセットuspto-grants-2014_02
ORD IDord-78bdd389d3534e50b6c0cd096fb8ef8e
出典メモuspto-grants-2014_02