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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 418679생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/418679

반응식

참여 물질

역할이름HCID투입량
반응물Methyl malonyl chlorideHCID 123460—
반응물2-Fluoro-N-methylanilineHCID 2759010—
용매DichloromethaneHCID 6344—
생성물Methyl 3-((2-fluorophenyl)(methyl)amino)-3-oxopropanoateHCID 58790179—

반응 조건

온도0 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093264B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-af84ee52720a4397ace7f65f3c8cb1d9
출처 메모uspto-grants-2012_01