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HRID 362665作成日:2026年10月26日

Sodium Azide → ethyl (S)-4-azido-3-hydroxybutyrate

https://huagongshe.com/reaction/362665

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium AzideHCID 33557—
反応物Ethyl (3S)-4-chloro-3-hydroxybutanoateHCID 7019277—
溶媒DimethylformamideHCID 6228—
生成物ethyl (S)-4-azido-3-hydroxybutyrateHCID 10888398—

反応手順

To a mixture of ethyl (S)-4-chloro-3-hydroxybutyrate (1 93 g, 1.16 mol, optical purity:98.5% ee) and N,N-dimethylformamide (1.4 Lit.) is added sodium azide (151 g, 2.32 mol) and the mixture was stirred at 100°-110° C. for 2 hours. After cooling N,N-dimethylformamide was distilled off and to the residue was added water (1 Lit.). The mixture was extracted with ethyl acetate and the extract was dried over magnesium sulfate. By distillation off ethyl acetate under vacuo, there is obtained ethyl (S)-4-azido-3-hydroxybutyrate as a crude product (206 g). Then the crude product was dissolved in methanol (1 Lit.) and to it 5% palladium-carbon (10 g) was added. The mixture was stirred for 17 hours at room temperature under a hydrogen atmosphere. After the reaction was over, palladium-carbon was filtered off and the solvent was distilled off under vacuo. The resulting product was recrystallized from acetone-water to give (S)-4-hydroxy-2-pyrrolidone (99 g, 0.98 mol, yield:84%) as a colorless crystalline solid. Optical purity:98.3% ee, Specific rotation:[α]D22 -57.6°(c=1.00, H2O).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05869694
出典データセットuspto-grants-1999_02
ORD IDord-71e6b906275546c6a3582fbc70047819
出典メモuspto-grants-1999_02