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Dodecanoyl chloride → 4-Dodecoyloxymethyl-3-phenyl-2-triethylsilylfuran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dodecanoyl chloride | HCID 8166 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 3-Phenyl-2-triethylsilyl-4-furanmethanol | HCID 15037150 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-Dodecoyloxymethyl-3-phenyl-2-triethylsilylfuran | HCID 15037151 | — |
反応手順
To a stirred solution of 3-phenyl-2-triethylsilyl-4-furanmethanol (345 mg, 1.20 mmol) and triethylamine (182 mg, 1.80 mmol) in tetrahydrofuran (15 ml) at 0 degrees under argon was added lauroyl chloride (786 mg, 3.60 mmol). This solution was allowed to warm gradually to room temperature. After stirring an additional 2 hours the white precipitate was filtered off. The filtrate was taken up into ethyl ether, washed with saturated ammonium chloride, saturated sodium bicarbonate, H2O and brine. Evaporation of the dried (magnesium sulfate) extracts gave an oil which was purified by flash chromatography on silica using 2% ethyl ether/hexanes to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05298633 |
| 出典データセット | uspto-grants-1994_03 |
| ORD ID | ord-e4827a66859341669dc5aab13a884a9c |
| 出典メモ | uspto-grants-1994_03 |