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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004105Generated: November 1, 2026

Ammonium formate → Methyl 2-amino-2-(4-fluorophenyl)acetate

https://huagongshe.com/reaction/1004105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant4-Fluoro-alpha-[(phenylmethyl)amino]benzeneacetic acid methyl ester hydrochlorideHCID 69360922—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
ProductMethyl 2-amino-2-(4-fluorophenyl)acetateHCID 1094311887%

Reaction Conditions

Temperature50 °C

Reaction Steps

4-Fluoro-α-[(phenylmethyl)amino]benzeneacetic acid methyl ester hydrochloride (12.2 kg, 39.4 moles) was added to a slurry of 10% palladium-on-carbon (1.2 kg) in isopropanol (50 L). Ammonium formate (5.0 kg, 79.4 moles) was added and the batch was heated to 50° C. Progress of the reaction was monitored by HPLC. The batch was filtered through Hyflo Supercel and the filter cake was washed with isopropanol (25 L). The filtrate was evaporated to low volume and flushed with isopropyl acetate (50 L). The residue was dissolved in isopropyl acetate (30 L) and washed with 5% aqueous potassium phosphate (40 L), followed by saturated aqueous sodium chloride (10 L). The solution was evaporated under vacuum to give 5.79 kg (87% yield) of racemic α-amino-4-fluorobenzeneacetic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048859
Source datasetuspto-grants-2000_04
ORD IDord-6562638b21e2465a93540bbe4b63d758
Source noteuspto-grants-2000_04