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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089522Generated: October 25, 2026

Sodium Chloride → 2-(4-Fluorophenyl)-2-methyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/reaction/1089522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
Reactant3-ThiophenecarboxaldehydeHCID 68135—
Reactant2-(4-Fluorophenyl)-2,5-dimethylfuran-3(2H)-oneHCID 15086704—
SolventEthanolHCID 702—
Product2-(4-Fluorophenyl)-2-methyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanoneHCID 5369929962%

Reaction Steps

To a solution of 3-thiophenecarboxaldehyde (1.3 g, 1.2 mM) and 2,5-dimethyl-2-(4-fluorophenyl)-3(2H)-furanone (2.0 g, 9.8 mM)in ethanol (75 mL), was added 1N aqueous sodium hydroxide (2 mL, 2 mM). The reaction solution was stirred at room temperature for one day. After saturated aqueous sodium chloride (400 mL) was added, the aqueous layer was extracted with dichloromethane (3×100 mL). The combined dichloromethane extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give a brown oil. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to afford a yellow solid (1.8 g, 62% yield), m.p. 97°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04966905
Source datasetuspto-grants-1990_10
ORD IDord-d1433dff9135464fa24e212e26497398
Source noteuspto-grants-1990_10