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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193043Generated: October 27, 2026

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

https://huagongshe.com/reaction/1193043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant(4-Bromo-2-ethylphenyl)furan-2-yl-methanolHCID 58070821—
SolventWaterHCID 962—
Product5-(4-Bromo-2-ethylphenyl)-4-hydroxycyclopent-2-enoneHCID 58070872—

Reaction Steps

To a solution of (4-bromo-2-ethylphenyl)furan-2-yl-methanol (13.6 g, 0.039 mol) in acetone (300 ml) and water (30 ml) at 55° C. is added polyphosphoric acid (5.0 g, 0.05 mol). After stirring at this temperature for 20 hours the reaction mixture is cooled to room temperature then concentrated in vacuo. The crude product is then partitioned between ethyl acetate (200 ml) and water (200 ml), and the organic phase is separated. After drying over anhydrous magnesium sulfate, all solvents are removed and the crude product is purified by flash column chromatography (1:1 ethyl acetate/hexane) to afford 5-(4-bromo-2-ethylphenyl)-4-hydroxycyclopent-2-enone as a brown gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680339B2
Source datasetuspto-grants-2014_03
ORD IDord-c0571d27379b4395afa8217af1f9509a
Source noteuspto-grants-2014_03