関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyl Chloride | HCID 7503 | — |
| 反応物 | 2-Butene-1,4-diol | HCID 8065 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 触媒 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 生成物 | 1,4-Bis(benzyloxy)-2-butene | HCID 4054109 | 114.5% |
反応手順
To 48% aqueous sodium hydroxide (127.8 g) was added tetra-n-butylammonium bromide (3.3 g, 10 mmol). The mixture was heated to 60° C. To the mixture was added 2-butene-1,4-diol (17) (30.0 g, 340 mmol), to which was added dropwise benzyl chloride (94.8 g, 743 mmol) at 80±15° C. The mixture was stirred at the same temperature for 2 hours. The reaction mixture was cooled down, and separated after the addition of water (90 ml). To the organic layer was added sulfuric acidic brine. The solution was neutralized by aqueous sodium hydrogen carbonate, separated, mixed with ethyl acetate and concentrated under reduced pressure to yield the objective (18) (104.5 g, quantitative) as an oil residue.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07087764B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-4caad36be5ac4269aa3917d91c05067e |
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| 出典メモ | uspto-grants-2006_08 |
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