참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| 반응물 | (R)-3-(benzyloxy)propane-1,2-diol | HCID 2724795 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (S)-1-Benzyloxy-3-(t-butyldiphenylsilyloxy)propan-2-ol | HCID 10982698 | 90% |
반응 단계
To a solution of (R)-3-benzyloxypropane-1,2-diol (prepared from (S)-4-benzylymethyl-2,2-dimethyl-1,3-dioxolane (commercially available from FLUKA) by acid hydrolysis using 80% aqueous acetic acid), (8.3 g, 47.2 mmol) in dry THF (70 ml) was added imidazole (6.42 g, 94.4 mmol). After 2 minutes, t-butyldiphenylsilyl chloride (12.28 ml, 47.2 mmol) was added. A white precipitate formed immediately. After 2 hours, the reaction mixture was filtered and the filtrate evaporated. The residue was partitioned between ethyl acetate and water, the organic layer separated, washed with saturated brine, dried (MgSO4), filtered and evaporated to give a colourless oil. Chromatography of the oil on silica gel (dichloromethane as eluant) afforded the title compound as a colourless oil (17.72 g, 90%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05247085 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-cf9e57ba9a5d488b84ad34a0e5f55896 |
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| 출처 메모 | uspto-grants-1993_09 |
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