참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzyl Alcohol | HCID 244 | — |
| 반응물 | Magnesium perchlorate | HCID 24840 | — |
| 반응물 | 3,6-Dioxabicyclo[3.1.0]hexane | HCID 67511 | — |
| 용매 | Isobutyronitrile | HCID 6559 | — |
| 생성물 | trans-3-Benzyloxy-4-hydroxytetrahydrofuran | HCID 14307979 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06140516 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-6b610ebf91754880a244f3c223e634ad |
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| 출처 메모 | uspto-grants-2000_10 |
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