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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650957Generated: November 2, 2026

Ethyl bromoacetate → Ethyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]acrylate

https://huagongshe.com/reaction/1650957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Chlorophenyl)cyclobutanecarbonitrileHCID 98621—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]acrylateHCID 67945594—

Reaction Steps

A suspension of zinc dust (25.5 g) (which had been activated by treatment with excess 3N hydrochloric acid followed by washing with water, ethanol and ether and drying) in dry tetrahydrofuran (250 ml) was stirred and heated under reflux while ethylbromoacetate (5 ml) was added dropwise. Stirring was continued for 15 minutes and 1-(4-chlorophenyl)cyclobutanecarbonitrile (15 g) was added. The mixture was heated under reflux and ethyl bromoacetate (60 g) was added over a period of 1 hour and the heating continued for a further 15 minutes. The mixture was then cooled and tetrahydrofuran (700 ml) and 25% aqueous potassium carbonate solution (300 ml) were added and the mixture was stirred for 15 minutes. The aqueous phase of the reaction mixture was separated, extracted with ether and the extracts combined with the organic phase of the reaction mixture, washed with brine and dried. Removal of the solvents gave an oil which was extracted with petroleum ether (b.p. 40°-60° C.). Removal of the solvent by evaporation gave ethyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]acrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925879
Source datasetuspto-grants-1990_05
ORD IDord-9daf99d50a9a4165ada0ada971e3f0e7
Source noteuspto-grants-1990_05