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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917579Generated: November 2, 2026

Hydrochloric Acid → (3-Cyanophenylamino)-2-fluorophenylacetic acid

https://huagongshe.com/reaction/917579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromobenzonitrileHCID 23381—
ReactantIodide IonHCID 30165—
Reactant2-Fluoro-DL-phenylglycineHCID 580073—
CatalystCopperHCID 23978—
SolventDimethylacetamideHCID 31374—
Product(3-Cyanophenylamino)-2-fluorophenylacetic acidHCID 58962742—

Reaction Conditions

Temperature90 °C

Reaction Steps

6.5 g (47.0 mmol) of potassium carbonate and 597 mg (3.10 mmol) of copper(l) iodide are added to a solution of 5.70 g (31.3 mmol) of 3-bromobenzonitrile and 5.30 g (31.3 mmol) of 2-fluoro-dl-alpha-phenylglycine in 30 ml of N,N-dimethylacetamide, and the mixture is stirred at 90° C. for 48 hours. The reaction mixture is then poured into 80 ml of 1N HCl and extracted twice with diethyl ether. The combined organic phases are extracted twice with 50 ml of 1N NaOH each time. The two basic aqueous phases are combined, acidified using 25% HCl and extracted twice with 80 ml of diethyl ether each time. These two organic phases are combined, dried using sodium sulfate and subsequently evaporated, giving (3-cyanophenylamino)-2-fluorophenylacetic acid as a yellowish solid; ESI 270.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273867B2
Source datasetuspto-grants-2007_09
ORD IDord-d0e550f080fe4e90b59eb0eba4289ec8
Source noteuspto-grants-2007_09