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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 418679Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl malonyl chlorideHCID 123460—
Edukt2-Fluoro-N-methylanilineHCID 2759010—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 3-((2-fluorophenyl)(methyl)amino)-3-oxopropanoateHCID 58790179—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093264B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-af84ee52720a4397ace7f65f3c8cb1d9
Quellennotizuspto-grants-2012_01