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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407843Generated: October 30, 2026

Acetone → 5-(2,4,6-Trimethylphenyl)-4-hydroxycyclopent-2-enone

https://huagongshe.com/reaction/407843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant(2,4,6-Trimethylphenyl)furan-2-ylmethanolHCID 49962474—
SolventWaterHCID 962—
Product5-(2,4,6-Trimethylphenyl)-4-hydroxycyclopent-2-enoneHCID 66684008—

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of (2,4,6-trimethylphenyl)furan-2-ylmethanol (27.8 g, 129 mmol) in acetone (730 ml) and water (100 ml) is heated to 55° C. and polyphosphoric acid (2 g) is added. The mixture is stirred at 55° C. for 7 hours, then cooled to room temperature overnight. 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-(2,4,6-trimethylphenyl)-4-hydroxycyclopent-2-enone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754242B2
Source datasetuspto-grants-2014_06
ORD IDord-03a80a937a0041a3a44d7c9afb53b33b
Source noteuspto-grants-2014_06