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Sodium Carbonate → 4-Ethoxybut-2-yn-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 反応物 | 2-(4-Ethoxy-but-2-ynyloxy)-tetrahydro-pyran | HCID 68529463 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-Ethoxybut-2-yn-1-ol | HCID 12786810 | 385.9% |
| 生成物 | Methyl acetate hexane | HCID 23449302 | 1% |
反応手順
To a solution of 2-(4-ethoxy-but-2-ynyloxy)-tetrahydro-pyran (0.5 g, 2.52 mmol) in methanol (10 mL) was added p-toluenesulfonic acid monohydrate (p-TSOH) (0.086 g, 0.454 mmol). The reaction mixture was stirred at room temperature for 3.5 hours. The reaction mixture was poured into aqueous sodium carbonate and extracted with methyl acetate. The organic layers were combined, dried (Na2SO4) and concentrated. Silica gel chromatography (1-10% MeOAc/hexane) provided 0.2 g of 4-ethoxy-but-2-yn-1-ol as a clear oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08642603B2 |
| 出典データセット | uspto-grants-2014_02 |
| ORD ID | ord-04be88845d1f4d6d9b54e5d1406b7d8f |
| 出典メモ | uspto-grants-2014_02 |