戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 487201作成日:2026年10月26日

Acrylonitrile → 6-fluoro-2,3-dihydro-4-cyano-4-[(trimethylsilyl)oxy]-4H-benzopyran

https://huagongshe.com/reaction/487201

反応式

関与物質

役割名称HCID仕込み量
反応物AcrylonitrileHCID 7855—
反応物4-FluorophenolHCID 9732—
反応物Trimethylsilyl cyanideHCID 82115—
反応物6-fluoro-2,3-dihydro-4H-1-benzopyran-4-oneHCID 2733262—
触媒zinc(II)iodideHCID 9883512—
溶媒DichloromethaneHCID 6344—
生成物6-fluoro-2,3-dihydro-4-cyano-4-[(trimethylsilyl)oxy]-4H-benzopyranHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05294635
出典データセットuspto-grants-1994_03
ORD IDord-70aed26fa3894f3d9b9329d82e6b201c
出典メモuspto-grants-1994_03