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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639304Generated: October 27, 2026

Ammonia → Ethyl N-(2-carbamoyl-5-chlorophenyl)aminoacetate

https://huagongshe.com/reaction/1639304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloroisatoic anhydrideHCID 329105—
SolventDimethylformamideHCID 6228—
ProductEthyl N-(2-carbamoyl-5-chlorophenyl)aminoacetateHCID 11780149—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 7-chloro-2H-3,1-benzoxazine-2,4(1H)-dione (330 g) in N,N-dimethylformamide (3.3 l) was added sodium hydride (60% in mineral oil, 86.8 g) below 20° C. and the mixture was stirred at 5° C. for 30 minutes. To this solution was added ethyl bromoacetate (222 ml) at 10° C. over a 30-minute period and the resulting mixture was stirred at room temperature for 1.5 hours. To this reaction mixture was added 28% aqueous ammonia (696 ml) below 10° C. and the resulting mixture was stirred at 5° C. for 20 minutes. The mixture was poured into 1N hydrochloric acid (16.5 l). The precipitates were collected by filtration, and washed in turn with water (3 times) and diethyl ether to give ethyl N-(2-carbamoyl-5-chlorophenyl)aminoacetate (360 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04883800
Source datasetuspto-grants-1989_11
ORD IDord-c8455e6407f94cd08801fdef87410b19
Source noteuspto-grants-1989_11