참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxiranemethanol, 3-[(phenylmethoxy)methyl]- | HCID 3934498 | — |
| 반응물 | HCID 178418473 | HCID 178418473 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Allyl-4-(benzyloxy)-3-hydroxy-1-butanol | HCID 18944106 | — |
반응 단계
A solution of 4-benzyloxy-2,3-epoxy-1-butanol (6.28 g, 32.37 mmol) in anhydrous tetrahydrofuran (75 mL) was added dropwise at -40° C. over a period of 45 minutes, to a 2M solution of allyl magnesium chloride (48.5 mL, 97 mmol) and tetrahydrofuran (50 mL). The solution was stirred at -40° C. for 1 hour, warmed to 0° C. and quenched by addition of aqueous ammonium chloride solution. The tetrahydrofuran layer was separated and the aqueous layer was extracted with ethyl acetate (three times). The combined organic extract was dried (magnesium sulfate), filtered and concentrated to obtain a mixture of compounds A and B.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05827868 |
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| 출처 데이터셋 | uspto-grants-1998_10 |
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| ORD ID | ord-757e5a1c8b554ab7918a14250606dd48 |
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| 출처 메모 | uspto-grants-1998_10 |
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