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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993902Generated: October 30, 2026

Ethyl bromoacetate → [(3-Chloro-phenyl)-methyl-amino]-acetic acid ethyl ester

https://huagongshe.com/reaction/1993902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium CarbonateHCID 10340—
Reactant3-chloro-N-methylanilineHCID 138900—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product[(3-Chloro-phenyl)-methyl-amino]-acetic acid ethyl esterHCID 6853623064.2%

Reaction Steps

To a solution of 3-chloro-N-methylaniline (0.50 g, 3.35 mmol) in ethanol (7 ml) were added sodium carbonate (0.53 g, 5.03 mmol) and ethyl bromoacetate (0.42 ml, 3.69 mmol). The resulting suspension was stirred at room temperature for 1 hour and was then heated at 100° C. for 15 min under microwave irradiation. The mixture was then cooled to room temperature, diluted with ether, and filtered. The filtrate was washed with 1 M aqueous hydrochloric acid, the phases separated, and the aqueous phase extracted with ether. The combined organic extracts were dried over sodium sulphate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (SiO2: heptane/ethyl acetate=gradient 100:0-70:30) to yield a brown oil (0.49 g, 64%); MS (ISP): 230.3, 228.1 ([M+H]+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652055B2
Source datasetuspto-grants-2010_01
ORD IDord-d44f30d20fe34b8a94fc1f82d97dc80c
Source noteuspto-grants-2010_01