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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380287Generated: November 1, 2026

Ethyl bromoacetate → 1-ethoxycarbonylmethyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole

https://huagongshe.com/reaction/2380287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantEthyl AcetateHCID 8857—
Reactant2,3-Dihydro-1H-imidazo(1,2-b)pyrazoleHCID 242471—
ReactantPotassium BicarbonateHCID 516893—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product1-ethoxycarbonylmethyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazoleHCID 18955294—

Reaction Steps

To a solution of 2,3-dihydro-1H-imidazo[1,2-b]-pyrazole (19 g) in dimethylsulfoxide (95 ml) were added ethyl bromoacetate (20.4 ml) and potassium bicarbonate (30 g) under ice-cooling. The mixture was stirred at room temperature for 4 hours. The reaction mixture was poured into a mixture of ethyl acetate (1.5 l) and water (500 ml). The separated organic layer was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated and the residue was subjected to column chromatography on silica gel using ethyl acetate as an eluent. Fractions containing the object compound were combined and evaporated in vacuo to give 1-ethoxycarbonylmethyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole (20.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05366970
Source datasetuspto-grants-1994_11
ORD IDord-b1aa8e6d07a0421ca12b5c590f597c0a
Source noteuspto-grants-1994_11