Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485435Generated: November 1, 2026

Ammonium Chloride → Methyl 3-(2-amino-4-fluorophenylamino)-2-methylpropanoate

https://huagongshe.com/reaction/1485435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 3-(4-fluoro-2-nitrophenylamino)-2-methylpropanoateHCID 70978244—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
ProductMethyl 3-(2-amino-4-fluorophenylamino)-2-methylpropanoateHCID 8671850481%

Reaction Steps

To a solution of methyl 3-(4-fluoro-2-nitrophenylamino)-2-methylpropanoate (14.0 g, 54.6 mmol) in ethanol (250 mL) were added zinc powder (14.2 g, 218 mmol) and saturated ammonium chloride (28.4 mL) at 0° C. Once addition was completed, the reaction mixture was stirred at reflux for 1 hour. Then the mixture was cooled to room temperature, filtered, and washed with ethanol (200 mL). The organic phase was concentrated in vacuo, dissolved in water (250 mL), and extracted with ethyl acetate (200 mL*3). The combined organic layers was separated, dried over anhydrous sodium sulfate, and concentrated to give a residue. The residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=2:1) to afford methyl 3-(2-amino-4-fluorophenylamino)-2-methylpropanoate as a black solid (10.0 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422292B2
Source datasetuspto-grants-2016_08
ORD IDord-7ecca4a3beff4a488eef176959f172b2
Source noteuspto-grants-2016_08