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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902644Generated: October 30, 2026

Methyl bromoacetate → [4-(3-Methoxy-phenyl)-piperidin-1-yl]-acetic Acid Methyl Ester

https://huagongshe.com/reaction/902644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(3-Methoxyphenyl)piperidineHCID 10702890—
SolventMethanolHCID 887—
Product[4-(3-Methoxy-phenyl)-piperidin-1-yl]-acetic Acid Methyl EsterHCID 6925293691%

Reaction Steps

A mixture of 4-(3-Methoxy-phenyl)-piperidine (0.8 g, 4.2 mmol), methylbromoacetate (1.28 g, 8.38 mmol), diisopropylethylamine (3.7 mL, 21 mmol) and MeOH (40 mL) was refluxed for 3 h. The reaction mixture was concentrated in vacuo, and the residue was partitioned between water and EtOAc and extracted. The organic layer was washed with water, brine, dried and concentrated in vacuo to give the title compound as an oil (1.0 g, 91% yield). MS(ESI) 264.2 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365085B2
Source datasetuspto-grants-2008_04
ORD IDord-1ae15fdc37d54ce7b0490ad22c5ef0c8
Source noteuspto-grants-2008_04