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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382184Generated: November 4, 2026

Ethyl bromoacetate → HCID 68735485, compound

https://huagongshe.com/reaction/2382184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTriethylamineHCID 8471—
ReactantHCID 68733876HCID 68733876—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 68735485HCID 6873548573%

Reaction Steps

To solution of N-phenyl-N-(3-(trifluoromethyl)phenyl)piperidin-4-amine (1.3 g, 4.1 mmol) in MeCN (15 mL) was added ethyl bromoacetate (0.50 ml, 4.5 mmol) followed by triethylamine (1.1 ml, 8.1 mmol). The reaction mixture was stirred at RT for 4 h, diluted with water and extracted with DCM. The combined DCM layer was dried (Na2SO4), and concentrated. The product was purified with ISCO using 0-15% EtOAc in DCM to give ethyl 2-(4-(phenyl(3-(trifluoromethyl)phenyl)amino)piperidin-1-yl)acetate (1.2 g, 73% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258306B2
Source datasetuspto-grants-2012_09
ORD IDord-214871f427b2423c88dc0dd10ae397a8
Source noteuspto-grants-2012_09