関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodoethane | HCID 6340 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol | HCID 11123315 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Methyl acetate hexane | HCID 23449302 | 1% |
| 生成物 | 2-(4-Ethoxy-but-2-ynyloxy)-tetrahydro-pyran | HCID 68529463 | — |
反応手順
An oven dried 500 ml RBF was charged with NaH (60% in mineral oil) (1.41 g, 35.3 mmol) and suspended in DMF (100 mL). The mixture was cooled to 0° C. and 4-(tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol (prepared in accordance with the procedures of Tamaru et al., Bull. Chem. Soc. Jpn., 1995, 1689-1705) (6.0 g, 35.3 mmol) was added. The reaction mixture was allowed to reach room temperature and stirred for one hour. To the mixture was added iodoethane (20.8 g, 133 mmol). The reaction mixture was stirred for 3.5 hours at room temperature before being quenched with ice/H2O and extracted with MeOAc. The organic phase was washed with brine, dried (Na2SO4) and concentrated. Silica gel chromatography (1-20% MeOAc/hexane) provided 4.71 g of 2-(4-ethoxy-but-2-ynyloxy)-tetrahydro-pyran as a clear oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08642603B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-fd436759d4e74f2f98770a0ccab266a0 |
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| 出典メモ | uspto-grants-2014_02 |
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