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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358965Generated: October 26, 2026

Acetic Acid → N-(2-Amino-4-bromophenyl)-2-chloroacetamide

https://huagongshe.com/reaction/2358965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium CarbonateHCID 10340—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-(4-bromo-2-nitrophenyl)-2-chloroacetamideHCID 16457083—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(2-Amino-4-bromophenyl)-2-chloroacetamideHCID 6691143343.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

Ferrous powder (19.8 g, 354 mmol), ammonium chloride (1.1 g, 19.7 mmol) and acetic acid (4.9 ml, 86.5 mmol) were suspended in 300 ml water and stirred at 50° C. for 15 min. To this mixture, a solution of N-(4-bromo-2-nitrophenyl)-2-chloroacetamide (11.5 g, 39.3 mmol) in 100 ml DMF was added quickly. After stirring for 15 min, the mixture was basified to pH 9 with aqueous sodium carbonate solution. The remaining solids were filtered and washed with water and ethyl acetate. Extraction of the water layer with ethyl acetate, washing of the combined organic layers with brine, drying over MgSO4, removing the solvent under reduced pressure and purification of the crude product by flash chromatography on silica gel (petroleum ether/ethyl acetate, 1/1) yielded N-(2-amino-4-bromophenyl)-2-chloroacetamide (4.5 g, 17.0 mmol, 43%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685960B2
Source datasetuspto-grants-2014_04
ORD IDord-3ca8dc5169c74aba8ef26f2003afa8ee
Source noteuspto-grants-2014_04