関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pentane | HCID 8003 | — |
| 反応物 | Heptyltriphenylphosphonium bromide | HCID 2724567 | — |
| 反応物 | 5-Benzyloxy-4-t-butyl-2-formylbenzofuran | HCID 23442879 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuran | HCID 54308722 | 91.2% |
反応手順
A pentane solution (2.6 ml, 4.2 mmol) of 1.6M n-butyllithium was added dropwise to a solution of n-heptyltriphenylphosphonium bromide (1.84 g, 4.2 mmol) in tetrahydrofuran (10 ml) under a nitrogen atmosphere. After stirring the mixture at room temperature for 30 min, a solution of 5-benzyloxy-4-tert-butyl-2-formylbenzofuran (1.0 g, 3.2 mmol) in tetrahydrofuran (10 ml) was added dropwise. Subsequently, the mixture was stirred at room temperature for 30 min, poured into ice water and subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and water, then dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica Gel chromatography (chloroform) to afford 5-benzyloxy-4-tert-butyl-2-(1-octenyl)benzofuran [1.14 g (yield, 91%)].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05663373 |
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| 出典データセット | uspto-grants-1997_09 |
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| ORD ID | ord-8f9839940081438eb9ea5381c16840c8 |
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| 出典メモ | uspto-grants-1997_09 |
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