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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1182120생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1182120

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Lithium borohydrideHCID 4148881—
반응물(S)-3-tert-Butoxycarbonylamino-4-methoxy-butyric acid benzyl esterHCID 57976545—
용매Diethyl EtherHCID 3283—
생성물tert-Butyl (S)-(4-hydroxy-1-methoxybutan-2-yl)carbamateHCID 53259998—

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07288537B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-21cdab5396d74da699493784cc7af339
출처 메모uspto-grants-2007_10