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HRID 380111作成日:2026年10月26日

Benzoin → (2R)-1-benzyloxycarbonyl-2-(4,5-diphenyloxazol-2-yl)pyrrolidine

https://huagongshe.com/reaction/380111

反応式

関与物質

役割名称HCID仕込み量
反応物BenzoinHCID 8400—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物2-DimethylaminopyridineHCID 21885—
反応物1-benzyl hydrogen (R)-pyrrolidine-1,2-dicarboxylateHCID 111208—
溶媒DichloromethaneHCID 6344—
生成物(2R)-1-benzyloxycarbonyl-2-(4,5-diphenyloxazol-2-yl)pyrrolidineHCID 54511676—

反応手順

To a solution of (2R)-N-benzyloxycarbonylproline (5 g) in CH2Cl2 (50 ml) were added benzoin (4.5 g), 1-ethyl 3-(3-dimethylaminopropyl)carbodiimide (3.9 ml), and dimethylaminopyridine (2.6 g) at room temperature under N2. After being stirred for 12 hours at room temperature, the solvent was evaporated in vacuo, and the residue was partitioned between ethyl acetate and water. The organic layer was washed with 1N-HCl solution, sat. NaHCO3, and brine, dried over MgSO4, and evaporated in vacuo. The obtained compound and CH3COONH4 (8.2 g) were dissolved in acetic acid (50 ml) and the mixture was stirred for 4 hours at 100° C. After the solvent was removed, the residue was partitioned between ethyl acetate and water. The organic layer was washed with water, sat. NaHCO3 and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give (2R)-1-benzyloxycarbonyl-2-(4,5-diphenyloxazol-2-yl)pyrrolidine (4 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06300344B1
出典データセットuspto-grants-2001_10
ORD IDord-286eda49468a416b9cc8faa1d2d8e88a
出典メモuspto-grants-2001_10