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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370317생성일: 2026년 10월 26일

Benzyl Alcohol → trans-3-Benzyloxy-4-hydroxytetrahydrofuran

https://huagongshe.com/reaction/370317

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물Magnesium perchlorateHCID 24840—
반응물3,6-Dioxabicyclo[3.1.0]hexaneHCID 67511—
용매IsobutyronitrileHCID 6559—
생성물trans-3-Benzyloxy-4-hydroxytetrahydrofuranHCID 14307979—

반응 조건

온도100 °C

반응 단계

To a flask fitted with a condenser and nitrogen inlet was added 3,4-epoxytetrahydrofuran (20 g, 0.23 mol), isobutyronitrile (100 ml, 5 vol), benzyl alcohol (124 g, 1.15 mol, 5 eq.) and finally magnesium perchlorate (10.3 g, 0.046 mol, 0.2 eq). The solution was heated at 100° C. for 24 hours. After cooling to room temperature, the reaction was quenched with water (1000 mL). The phases were separated and the aqueous phase was extracted with ethyl acetate (3×400 mL). After drying the organic phases over MgSO4, filtering and concentrating in vacuo, the trans-3-benzyloxy-4-hydroxytetrahydrofuran was isolated by column chromatography to give 29 g (66% yield) of a clear colorless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140516
출처 데이터셋uspto-grants-2000_10
ORD IDord-6b610ebf91754880a244f3c223e634ad
출처 메모uspto-grants-2000_10