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HRID 418679作成日:2026年10月25日

Methyl malonyl chloride → Methyl 3-((2-fluorophenyl)(methyl)amino)-3-oxopropanoate

https://huagongshe.com/reaction/418679

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl malonyl chlorideHCID 123460—
反応物2-Fluoro-N-methylanilineHCID 2759010—
溶媒DichloromethaneHCID 6344—
生成物Methyl 3-((2-fluorophenyl)(methyl)amino)-3-oxopropanoateHCID 58790179—

反応条件

温度0 °C

反応手順

To a solution of methyl 3-chloro-3-oxopropanoate (1.75 mL, 15.99 mmol) in dry DCM (32 ml) was added 2-fluoro-N-methylaniline (2 g, 15.99 mmol) and the reaction mixture was stirred at 0° C. for 1 h, evaporated then redissolved in EtOAc, washed with dilute NaHCO3, and brine. The organic phase was dried over sodium sulfate, and concentrated under reduced pressure to afford methyl 3-((2-fluorophenyl)(methyl)amino)-3-oxopropanoate as yellow oil which was used without further purification (3.3 g, 16 mmol, 97%, crude). To a solution of this material (3.3 g, 16 mmol) in THF (16 ml) and water (16 ml) was added LiOHH2O (1.35 g, 31.5 mmol) and the reaction mixture was stirred overnight, evaporated (to remove the THF) and then extracted with EtOAc. The aqueous phase was acidified to pH˜1 by addition of 1N HCl and extracted with EtOAc. The solution was dried over Na2SO4, filtered and concentrated under reduced pressure to afford the title compound 245 as a brown solid, which was used without further purification (2.75 g, 13.03 mmol, 81% yield). MS (m/z): (M+1) 218.0 (88%), (2M+Li) 429.0 (100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093264B2
出典データセットuspto-grants-2012_01
ORD IDord-af84ee52720a4397ace7f65f3c8cb1d9
出典メモuspto-grants-2012_01