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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110744Generated: November 1, 2026

Hydrochloric Acid → Ethyl 3-(bromophenyl)acetate

https://huagongshe.com/reaction/2110744

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 numberUS07517889B2
Source datasetuspto-grants-2009_04
ORD IDord-60713a3a94c44a2a8ad3565747bcfc84
Source noteuspto-grants-2009_04