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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428389Generated: November 2, 2026

Ethyl bromoacetate → HCID 117662380, compound

https://huagongshe.com/reaction/1428389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Benzoxazolinone, 5-(trifluoromethyl)-HCID 26852—
SolventAcetoneHCID 180—
ProductHCID 117662380HCID 117662380—

Reaction Steps

To a mixture of 5-trifluoromethyl-1,3-benzoxazol-2(3H)-one (999 mg) and acetone (25 mL) were added K2CO3 (1.02 g) and ethyl bromoacetate (708 μL) at room temperature, followed by heating to reflux for 4 hours. The reaction mixture was filtered while hot, and washed with acetone. The filtrate and the washed solution were combined and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: Hex/EtOAc=100/0-75/25) to obtain ethyl [2-oxo-5-(trifluoromethyl)-1,3-benzoxazol-3(2H)-yl]acetate (1.33 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937087B2
Source datasetuspto-grants-2015_01
ORD IDord-0d224dab88bc4eb0a24db75fe33c63e0
Source noteuspto-grants-2015_01