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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741423Generated: November 1, 2026

Ethyl bromoacetate → 1-[3-(Ethoxycarbonylmethoxy)benzoyl]-2-(4,5-diphenyl-2-oxazolyl)piperidine

https://huagongshe.com/reaction/1741423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-Hydroxybenzoyl)-2-(4,5-diphenyl-2-oxazolyl)piperidineHCID 18367315—
SolventAcetonitrileHCID 6342—
Product1-[3-(Ethoxycarbonylmethoxy)benzoyl]-2-(4,5-diphenyl-2-oxazolyl)piperidineHCID 1836724474.8%

Reaction Steps

A mixture of 1-(3-hydroxybenzoyl)-2-(4,5-diphenyl-2-oxazolyl)piperidine (100 mg), ethyl bromoacetate (61 mg), and K2CO3 (84 mg) in acetonitrile (1.0 ml) was stirred at room temperature overnight and partitioned between water and ethyl acetate. The organic layer was separated, washed with water and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford 1-[3-(ethoxycarbonylmethoxy)benzoyl]-2-(4,5-diphenyl-2-oxazolyl)piperidine (90 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972965
Source datasetuspto-grants-1999_10
ORD IDord-5130e6490eba410d84bb5605b211fdd7
Source noteuspto-grants-1999_10