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Acrylonitrile → 6-fluoro-2,3-dihydro-4-cyano-4-[(trimethylsilyl)oxy]-4H-benzopyran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acrylonitrile | HCID 7855 | — |
| 反応物 | 4-Fluorophenol | HCID 9732 | — |
| 反応物 | Trimethylsilyl cyanide | HCID 82115 | — |
| 反応物 | 6-fluoro-2,3-dihydro-4H-1-benzopyran-4-one | HCID 2733262 | — |
| 触媒 | zinc(II)iodide | HCID 9883512 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 6-fluoro-2,3-dihydro-4-cyano-4-[(trimethylsilyl)oxy]-4H-benzopyran | HCID 14339429 | — |
反応手順
To a solution of 20 g (0.12 moles) of 2,3,-dihydro-6-fluoro-4H-benzopyran-4-one (prepared from 4-fluorophenol and acrylonitrile as described in J. Med. Chem., 28, 1716 (1985) and 23 mL (0.18 moles) of trimethylsilyl cyanide in 220 mL of CH2Cl2 was added 500 mg of zinc iodide. The reaction was stirred at room temperature for 20 hours then poured onto ice-water. The CH2Cl2 layer was washed with water, 10% aqueous NaHCO3 and brine then dried over MgSO4, filtered and evaporated to give 32 g of crude product which was used without purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05294635 |
| 出典データセット | uspto-grants-1994_03 |
| ORD ID | ord-70aed26fa3894f3d9b9329d82e6b201c |
| 出典メモ | uspto-grants-1994_03 |