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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359357Generated: October 27, 2026

Sodium Hydroxide → 2,2-Dimethyl-5-[2-(4-fluorophenyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/reaction/359357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant3(2H)-Furanone, 2,2,5-trimethyl-HCID 137080—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventSodium ChlorideHCID 5234—
Product2,2-Dimethyl-5-[2-(4-fluorophenyl)ethenyl]-3(2H)-furanoneHCID 5450358260.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2,2,5-trimethyl-3(2H)-furanone (2.0 g, 15.9 mM) and 4-fluorobenzaldehyde (1.6 g, 13.2 mM) in ethanol (100 mL), was added 1N aqueous sodium hydroxide (1.6 mL, 1.6 mM). The reaction solution was heated at 50° C. for four hours. After the reaction solution was cooled to room temperature and diluted with saturated aqueous sodium chloride (200 mL) and water (200 mL), the aqueous solution was extracted with diethyl ether (2×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (25 mL), dried over magnesium sulfate, filtered and concentrated at reduced pressure to afford a dark yellow crystalline solid. The crude product was recrystallized from hexane to give light yellow crystals (1.8 g, 45% yield), m.p. 55°-57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001126
Source datasetuspto-grants-1991_03
ORD IDord-f7c4370264ef4afa9c17b83d3ff7a798
Source noteuspto-grants-1991_03