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HRID 1765636作成日:2026年10月26日

Lithium borohydride → (R)-Benzyl (1,5-dihydroxypentan-2-yl)carbamate

https://huagongshe.com/reaction/1765636

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium borohydrideHCID 4148881—
反応物Dimethyl (2R)-2-{[(benzyloxy)carbonyl]amino}pentanedioateHCID 86606597—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物(R)-Benzyl (1,5-dihydroxypentan-2-yl)carbamateHCID 275738290%

反応手順

A solution of dimethyl (2R)-2-{[(benzyloxy)carbonyl]amino}pentanedioate (22.4 g) in dry THF (74 ml) was added dropwise over 1 h to a stirred mixture of lithium borohydride (4.5 g) in THF (200 ml) at room temperature, under nitrogen. Stirring at room temperature was continued for 3 days. The reaction mixture was diluted with brine and water, and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give the title compound (16.5 g) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07226929B2
出典データセットuspto-grants-2007_06
ORD IDord-4fc5996bb36244dc8c309fd9c4e8d29e
出典メモuspto-grants-2007_06