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HRID 130315作成日:2026年10月25日

2,3,4,5-Tetrafluorobenzoyl chloride → Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoate

https://huagongshe.com/reaction/130315

反応式

関与物質

役割名称HCID仕込み量
反応物2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
反応物Potassium ethyl malonateHCID 3446434—
反応物Magnesium ChlorideHCID 5360315—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—

反応手順

Potassium ethyl malonate (3.66 g, 21.5 mmol), MgCl2 (2.44 g, 25.7 mmol) and TEA (2.05 g, 20.3 mmol) were mixed in acetonitrile (70 ml) at 10-15° C. for 2.5 hr. 2,3,4,5-tetrafluorobenzoyl chloride (2.00 g, 10.3 mmol) in acetonitrile (10 ml) was added at 0° C. over 15 min followed by a second addition of TEA (0.23 g, 2.3 mmol). After allowing to warm to RT, the mixture was stirred for 16 hr. After removal of volatiles in vacculo Toluene (30 ml) was added and removed in vacuo. Following the addition of toluene (60 ml), HCl 1.5 M (40 ml) was added cautiously, ensuring the temperature did not exceed 25° C. The organic fraction was washed with HCl 1.5 M (2×25 ml) and water (2×25 ml), dried over MgSO4 and reduced to a light orange oil in vacuo ([M+1]+265, 98%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381720B2
出典データセットuspto-grants-2008_06
ORD IDord-474bceeecd274ea987153a50a8377102
出典メモuspto-grants-2008_06