참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodoethane | HCID 6340 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol | HCID 11123315 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Methyl acetate hexane | HCID 23449302 | 1% |
| 생성물 | 2-(4-Ethoxy-but-2-ynyloxy)-tetrahydro-pyran | HCID 68529463 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642603B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-fd436759d4e74f2f98770a0ccab266a0 |
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| 출처 메모 | uspto-grants-2014_02 |
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