関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Propargyl bromide | HCID 7842 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 1,4-Benzenedimethanol | HCID 11506 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-[(2-Propynyloxy)methyl]benzyl alcohol | HCID 54520131 | 58% |
反応手順
To a mixture of sodium hydride (400 mg, 8.4 mmol, 50% in oil) and tetrahydrofuran (30 mL) was added 1,4-benzenedimethanol (2.3 g, 17 mmol) at 0° C., and then N,N-dimethylformamide (30 mL) was added. The reaction mixture was stirred at room temperature for 10 minutes, after which propargyl bromide (1.0 g, 8.4 mmol) was added dropwise to the reaction mixture at 0° C. The reaction mixture was stirred at room temperature for 1 hour, after which water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was washed and saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The residue thus obtained was purified by NH silica gel column chromatography (heptane:ethyl acetate=3:2) to obtain the title compound (860 mg, 58%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07691882B2 |
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| 出典データセット | uspto-grants-2010_04 |
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| ORD ID | ord-069a5b2d59254c22abe480ca278edf54 |
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| 出典メモ | uspto-grants-2010_04 |
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