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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323697Generated: October 28, 2026

Ethyl bromoacetate → 3-(10,11-Dihydro-5h-dibenz[b,f]azepin-5-ylmethyl)-1-piperidylacetic acid ethyl ester

https://huagongshe.com/reaction/323697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylcarbonyl)-1-benzylpiperidine hydrogen oxalate hemihydrateHCID 131722490—
SolventAcetoneHCID 180—
Product3-(10,11-Dihydro-5h-dibenz[b,f]azepin-5-ylmethyl)-1-piperidylacetic acid ethyl esterHCID 5383489487%

Reaction Steps

A mixture of the above piperidine (2.05 g, 7 mmol), ethyl bromoacetate (1.36 g, 8.1 mmol), potassium carbonate (1.7 g, 12.3 mmol) and acetone (50 ml) was heated at reflux temperature under stirring for 7 h. The mixture was filtered and the solvent evaporated in vacuo. The oily residue was purified on silica gel (20 g) using ethyl acetate as eluent to give 2.3 g (87%) 3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylmethyl)-1-piperidylacetic acid ethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214816B1
Source datasetuspto-grants-2001_04
ORD IDord-5205845a8cd64092b676e2771e162424
Source noteuspto-grants-2001_04