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Tetrahydrofuran → {[(2-Methylbut-3-yn-1-yl)oxy]methyl}benzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 生成物 | {[(2-Methylbut-3-yn-1-yl)oxy]methyl}benzene | HCID 59201193 | — |
反応手順
A solution of BuLi (4.32 ml, 6.92 mmol) (1.6M in hexanes) was added dropwise to a stirred solution of the dibromo alkene (above, 1.1 g, 3.29 mmol) in dry THF (15 ml) under N2, such that the internal temperature <−70° C. The reaction was stirred at this temperature for 30 minutes and then quenched with saturated aqueous ammonium chloride (1 ml) before being allowed to warm to RT. The mixture was partitioned between diethyl ether and water. The aqueous layer was extracted with diethyl ether (×2). The combined extracts were washed with brine (×1), dried (Na2SO4), filtered and evaporated. The residue was purified by chromatography (silica, 1-4% Et2O/isohexane) to give the alkyne (0.55 g) as a colourless liquid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08389547B2 |
| 出典データセット | uspto-grants-2013_03 |
| ORD ID | ord-16b5265af9704caf8e914ab8a1d0cdb4 |
| 出典メモ | uspto-grants-2013_03 |