関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Oxiranemethanol, 3-[(phenylmethoxy)methyl]- | HCID 3934498 | — |
| 反応物 | HCID 178418473 | HCID 178418473 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-Allyl-4-(benzyloxy)-3-hydroxy-1-butanol | HCID 18944106 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05827868 |
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| 出典データセット | uspto-grants-1998_10 |
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| ORD ID | ord-757e5a1c8b554ab7918a14250606dd48 |
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| 出典メモ | uspto-grants-1998_10 |
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