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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338395Generated: October 25, 2026

Ethanol → 1-(4-Bromophenyl)cyclobutane-1-carboxylic acid

https://huagongshe.com/reaction/338395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(4-Bromophenyl)cyclobutanecarbonitrileHCID 20111608—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(4-Bromophenyl)cyclobutane-1-carboxylic acidHCID 1676991979%

Reaction Steps

To a solution of 1-(4-bromophenyl)cyclobutanecarbonitrile (1.0 g, 4.2 mmol) in EtOH (28 mL) and water (2 mL) was added KOH (2.1 g, 42 mmol). The reaction mixture was heated to reflux for 16 hours. The reaction was then quenched with 1M hydrochloric acid in order to adjust pH to 7. The organic solvents were removed in vacuo to give a residue, which was dissolved in ethyl acetate (40 mL), then washed with brine (3×10 mL). The organic phase was concentrated in vacuo, and the resulting oil was purified by flash chromatography on silica gel (petroleum ether/ethyl acetate=8:1) to give 1-(4-bromophenyl)cyclobutanecarboxylic acid (0.8 g, 79% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-17a26f997c2c40908d3a5e55c854d700
Source noteuspto-grants-2014_11