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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216216Generated: October 30, 2026

Hydrochloric Acid → Ethyl 3-(bromophenyl)acetate

https://huagongshe.com/reaction/216216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant(3-Bromophenyl)acetic acidHCID 74653—
ProductEthyl 3-(bromophenyl)acetateHCID 1147055293.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

HCl is bubbled through a solution of 3-bromophenyl acetic acid (10.5 g, 46.5 mmol) in EtOH (70 mL) chilled at 0° C. for 5 minutes. The flask is capped and stirred at ambient temperature for 5 hours. The mixture is concentrated. The residue is taken up with water (80 mL) and extracted twice with EtOAc (70 mL). The organic extracts are combined and dried over magnesium sulfate, filtered and concentrated to afford (3-bromo-phenyl)-acetic acid ethyl ester [10.55 g, 93.4%] as an oil, which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193183B2
Source datasetuspto-grants-2012_06
ORD IDord-3ff37ecbdf284611b966ae6c2176dfa9
Source noteuspto-grants-2012_06