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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430757Generated: October 30, 2026

Acetone → 5-(5-Bromo-2-ethylphenyl)-4-hydroxycyclopent-2-enone

https://huagongshe.com/reaction/1430757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant(5-Bromo-2-ethylphenyl)furan-2-ylmethanolHCID 58061495—
SolventWaterHCID 962—
Product5-(5-Bromo-2-ethylphenyl)-4-hydroxycyclopent-2-enoneHCID 58061516—

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of (5-bromo-2-ethylphenyl)furan-2-ylmethanol (40.73 g, 0.145 mol) in acetone (1150 ml) and water (170 ml) is heated to 55° C. and 30 drops of polyphosphoric acid are added. The mixture is stirred at 55° C. for 44 hours, then cooled to room temperature. The reaction mixture is concentrated under reduced pressure to remove most of the acetone then ethyl acetate (500 ml) is added, and the reaction mixture is partitioned. The aqueous phase is extracted into ethyl acetate and the organic solutions are combined, washed with saturated aqueous sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate, filtered and the filtrate is concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to give 5-(5-bromo-2-ethylphenyl)-4-hydroxycyclopent-2-enone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940913B2
Source datasetuspto-grants-2015_01
ORD IDord-400e287696f946b7b9a451876525d946
Source noteuspto-grants-2015_01