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Tetrabutylammonium Fluoride → beta-Methylenephenethyl alcohol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 反応物 | tert-Butyl-dimethyl-(2-phenyl-allyloxy)-silane | HCID 67155247 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | beta-Methylenephenethyl alcohol | HCID 80106 | 99.8% |
反応手順
To a well stirred solution of tert-butyl-dimethyl-(2-phenyl-allyloxy)-silane (1.3 g, 5.23 mmol) in tetrahydrofuran (10 mL) is slowly added a solution of a 1 N tetrabutylammonium fluoride in tetrahydrofuran (10.5 mL, 10.5 mmol). The reaction is allowed to stir for 20 min, quenched by the addition of a saturated aqueous solution of ammonium chloride and extracted several times with ethyl acetate The organic layers are combined, washed with water, brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue is purified via silica gel chromatography (10% ethyl acetate in hexanes) to yield 700 mg of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08841291B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-040cf4c5b67048c3a151c517cf90500a |
| 出典メモ | uspto-grants-2014_09 |