戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2078055作成日:2026年10月25日

Diethyl Malonate → Diethyl 2-(2-(4-fluorophenyl)-2-methylpropanoyl)malonate

https://huagongshe.com/reaction/2078055

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl MalonateHCID 7761—
反応物Magnesium ChlorideHCID 5360315—
反応物2-(4-Fluorophenyl)-2-methylpropanoic acidHCID 20163803—
溶媒AcetonitrileHCID 6342—
溶媒Thionyl ChlorideHCID 24386—
生成物Diethyl 2-(2-(4-fluorophenyl)-2-methylpropanoyl)malonateHCID 6709982496.3%

反応条件

温度0 °C

反応手順

A mixture of diethyl malonate (3 g, 16 mmol) in 50 mL ACN was stirred at 0° C., was treated with MgCl2 (2 g, 18 mmol) in one portion, and was treated dropwise with TEA (3 g, 33 mmol). The mixture was stirred at room temperature for 2.5 hours. A mixture of 2-(4-fluorophenyl)-2-methylpropanoic acid (3 g, 16 mmol) in thionyl chloride (20 mL) was refluxed for 2 hours and then concentrated in vacuo. The residue was diluted with 10 mL ACN, and was added dropwise to the above mixture. The mixture was stirred at 50° C. for 15 hours. The resulting mixture was then cooled to room temperature, diluted with 100 mL ether, washed with H2O (2×50 mL) and brine 20 mL, dried over anhydrous Na2SO4, and concentrated in vacuo. The crude product was purified by column chromatography eluting with 10-20% EtOAc/hexane to give 5 g of the product as pale yellow oil. MS m/e=325 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07928139B2
出典データセットuspto-grants-2011_04
ORD IDord-18c0cb6cc0984bc99a5effa35e620067
出典メモuspto-grants-2011_04