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HRID 1182120作成日:2026年10月25日

Tetrahydrofuran → tert-Butyl (S)-(4-hydroxy-1-methoxybutan-2-yl)carbamate

https://huagongshe.com/reaction/1182120

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Lithium borohydrideHCID 4148881—
反応物(S)-3-tert-Butoxycarbonylamino-4-methoxy-butyric acid benzyl esterHCID 57976545—
溶媒Diethyl EtherHCID 3283—
生成物tert-Butyl (S)-(4-hydroxy-1-methoxybutan-2-yl)carbamateHCID 53259998—

反応手順

A solution of (S)-3-tert-Butoxycarbonylamino-4-methoxy-butyric acid benzyl ester (10.4 g, 32.3 mmol) in dry diethylether (70 ml) cooled to 0° C. is treated slowly with a 2.0 M solution of LiBH4 in THF (32.2 ml, 64.4 mmol). The reaction mixture is allowed to warm to ambient temperature and then left to stir. After 6 hours the reaction mixture is quenched slowly with 0.5 M aqueous solution of citric acid and extracted with ether. The ether phase is dried over magnesium sulphate and evaporated. The crude product is purified by flash silica chromatography (elution with a gradient 3:7 to 6:4 ethylacetate/hexane) to afford ((S)-3-Hydroxy-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester as a clear oil. [M-BOC] 120.13

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07288537B2
出典データセットuspto-grants-2007_10
ORD IDord-21cdab5396d74da699493784cc7af339
出典メモuspto-grants-2007_10