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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980618Generated: October 25, 2026

Acetic Acid → 2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propen-1-yl)-

https://huagongshe.com/reaction/1980618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium ChlorideHCID 5234—
ReactantSodium AcetateHCID 517045—
Reactant5-Methyl-2-furylallylcarbinolHCID 70478334—
SolventWaterHCID 962—
Product2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propen-1-yl)-HCID 11083219.8%

Reaction Steps

A buffer solution was prepared by dissolving sodium acetate (1.03 g) and Paion D-408 (polyoxyethylene alkyl phenyl ether; manufactured by Takemoto Yushi Inc.) (0.44 g) in water (200 ml) and adjusting the pH value to 6.0 with acetic acid. In a reaction vessel, 5-methyl-2-furylallylcarbinol (5 g) and the entire amount of the buffer solution as prepared above were charged, and the temperature was elevated up to 150° C. in 35 minutes while stirring. The mixture was stirred at the same temperature for 3.5 hours. After ice-cooling, sodium chloride (50 g) was added, and the mixture was extracted with methyl isobutyl ketone (100 ml) four times. The extract was concentrated at 60° C. under reduced pressure to remove methyl isobutyl ketone, whereby an oily substance (4.6 g) was obtained. The crude product was purified by column chromatography with silica gel (60 g) (developing solvent, ethyl acetate-n-hexane (1:2 by volume)) to obtain 2-allyl-3-methyl-4-hydroxy-2-cyclopentenone (4.2 g). Yield, 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510329
Source datasetuspto-grants-1985_04
ORD IDord-4b7e38ede6874f5e84f6cdb7e994f323
Source noteuspto-grants-1985_04