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HRID 1021365作成日:2026年10月26日

Ethyl Acetate → 7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromene-4-carboxylic acid

https://huagongshe.com/reaction/1021365

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Trimethylsilyl cyanideHCID 82115—
反応物7-fluoro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-oneHCID 15205373—
触媒zinc(II)iodideHCID 9883512—
溶媒Hydrochloric AcidHCID 313—
生成物7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromene-4-carboxylic acidHCID 6708039424.25%

反応条件

温度50 °C

反応手順

To 7-fluoro-2,2-dimethyl-2,3-dihydrochromen-4-one (1.000 g, 5.149 mmol) was added trimethylsilyl cyanide (3.215 mL, 25.75 mmol) followed by a spatula tip of zinc iodide. The reaction was heated at 50° C. for 1 hour. The reaction was cooled, diluted with ethyl acetate (40 mL) and washed with saturated sodium bicarbonate (2×25 mL), brine (25 mL), dried over magnesium sulfate and concentrated. The product was dissolved in 5 mL of acetic acid and 5 mL of HCl, and SnCl2 dihydrate (4.648 g, 20.60 mmol) was added. The reaction heated at reflux (130° C. oil bath temperature) overnight. The reaction was cooled, diluted with ethyl acetate (50 mL), washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate and concentrated. The residue was purified by silica gel chromatography over silica gel eluting with a gradient of 0.5% MeOH/CH2Cl2 containing 0.5% acetic acid to 10% MeOH/CH2Cl2 containing 0.5% acetic acid to provide the title compound (0.280 g, 24.25% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08716498B2
出典データセットuspto-grants-2014_05
ORD IDord-150d4e245b7741a38f0706ab981a186d
出典メモuspto-grants-2014_05