Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967322Generated: October 25, 2026

Ethyl Acetate → N-(3-chloro-4-cyanophenyl)-4-fluorophenylalanine

https://huagongshe.com/reaction/1967322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant2-Chloro-4-fluorobenzonitrileHCID 109000—
Reactant4-fluoro-L-phenylalanineHCID 716312—
SolventDimethyl SulfoxideHCID 679—
ProductN-(3-chloro-4-cyanophenyl)-4-fluorophenylalanineHCID 67105225100.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 2-chloro-4-fluorobenzonitrile (1.8 g) in dimethyl sulfoxide (30 mL) were added 4-fluorophenylalanine (2.54 g) and cesium carbonate (4.90 g), and the mixture was stirred at 90° C. overnight. After allowing to room temperature, ethyl acetate was added, and the mixture was extracted twice with saturated aqueous sodium hydrogen carbonate solution. The aqueous layers were combined, and acidified with citric acid, and the mixture was extracted twice with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound as a brown oil (yield: 3.69 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420694B2
Source datasetuspto-grants-2013_04
ORD IDord-1c3b502b23944b5ab5ce0b2610de398a
Source noteuspto-grants-2013_04