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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668744Generated: October 31, 2026

Ethanol → 3-Bromo-5-ethoxybenzoic acid

https://huagongshe.com/reaction/1668744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57825009HCID 57825009—
SolventWaterHCID 962—
Product3-Bromo-5-ethoxybenzoic acidHCID 53217019—

Reaction Steps

A solution of 3-bromo-5-ethoxy-benzonitrile (529 mg, 2.3 mmol) in a mixture of ethanol (8 mL) and water (1 mL) was treated with a solution of sodium hydroxide (47%, 0.66 mL) and the mixture heated under reflux for 1 hour. For the working-up, the mixture was evaporated under reduced pressure and the oily residue dissolved in tert-butylmethyl ether (60 mL) and water (30 mL). The organic layer was separated and evaporated, then treated again with tert-butylmethyl ether (120 mL) and 1 N hydrochloric acid (60 mL). The organic layer was separated and re-extracted twice with tert-butylmethyl ether (2×60 mL). The organic layers were combined, washed with brine, dried over sodium sulfate, and evaporated under reduced pressure. The title compound was obtained in quantitative yield and engaged in the next step without further purification. Mass (calculated) C9H9BrO3 [244]; (found) [M−H]+=243, 245.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989449B2
Source datasetuspto-grants-2011_08
ORD IDord-32f30f88ea33405fb4038f91929b08e9
Source noteuspto-grants-2011_08