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HRID 352573作成日:2026年10月25日

Sodium borohydride → 5-(3-Hydroxy4-phenyl-butyl)-pyrrolidin-2-one

https://huagongshe.com/reaction/352573

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物5-(3-Oxo-4-phenyl-butyl)-pyrrolidin-2-oneHCID 12970083—
溶媒EthanolHCID 702—
生成物5-(3-Hydroxy4-phenyl-butyl)-pyrrolidin-2-oneHCID 1297008472.2%

反応条件

温度0 °C

反応手順

To a solution of 5-(3-oxo-4-phenyl-butyl)-pyrrolidin-2-one (5.902 g, 25.52 mmol) in EtOH (30 mL) at 0° C. was added NaBH4 (485 mg, 12.76 mmol) and the reaction mixture was stirred at 0° C. for 2.5 h. The reaction mixture was quenched with saturated aqueous ammonium chloride. Water and CH2Cl2 were added. The aqueous layer was washed with CH2Cl2 (2×) and the combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was purified by medium pressure chromatography with a solvent gradient (1:1 hexanes:EtOAc to EtOAc to 1% MeOH in CH2Cl2) to yield 4.3 g of 5-(3-hydroxy-4-phenyl-butyl)-pyrrolidin-2-one. 1H NMR (CDCl3) δ7.35-7.16 (m, 5H), 6.02 (m, 1H), 3.80 (m, 1H), 3.63 (m, 1H), 2.79 (m, 1H), 2.64 (m, 1H), 2.26 m, 3H), 1.72-1.22 (m, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747054B2
出典データセットuspto-grants-2004_06
ORD IDord-3ef5d39fdb46413aaf9c080b8e0cdf0e
出典メモuspto-grants-2004_06