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HRID 1527912作成日:2026年10月27日

Hexachloroethane → (2S,4R)-4-tert-butoxy-2-oxazol-2-yl-pyrrolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1527912

反応式

関与物質

役割名称HCID仕込み量
反応物HexachloroethaneHCID 6214—
反応物TriethylamineHCID 8471—
反応物TriphenylphosphineHCID 11776—
反応物(2S,4R)-4-tert-butoxy-2-(2-oxo-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl esterHCID 59548499—
溶媒DichloromethaneHCID 6344—
生成物(2S,4R)-4-tert-butoxy-2-oxazol-2-yl-pyrrolidine-1-carboxylic acid benzyl esterHCID 5954849246.7%

反応条件

温度0 °C

反応手順

To a stirred solution of (2S,4R)-4-tert-butoxy-2-(2-oxo-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester (4.5 g, 12.43 mmol) and hexachloroethane (5.88 g, 24.86 mmol) in dichloromethane (30 mL) was added triphenyl phosphine (6.52 g, 24.86 mmol) The mixture was stirred at 0° C. for 15 min, triethylamine (2.5 g, 24.86 mmol) was then added and the mixture was stirred at room temp. for 14 h. The reaction mixture was then extracted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by column chromatography (using 15% EtOAc in hexane as eluent) to give (2S,4R)-4-tert-butoxy-2-oxazol-2-yl-pyrrolidine-1-carboxylic acid benzyl ester (2 g, 46.6% yield) as a yellow liquid. MS calcd. for C19H25N2O4 [(M+H)+] 345.0, obsd. 345.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09090559B2
出典データセットuspto-grants-2015_07
ORD IDord-0a1694a9d5c4432f8ad7a09c31456988
出典メモuspto-grants-2015_07