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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085589Generated: October 25, 2026

Sodium Chloride → 2-Methyl-2-(4-fluorophenyl)-5-[2-(2-pyridinyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/reaction/1085589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant2-PyridinecarboxaldehydeHCID 14273—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-(4-Fluorophenyl)-2,5-dimethylfuran-3(2H)-oneHCID 15086704—
SolventEthanolHCID 702—
Product2-Methyl-2-(4-fluorophenyl)-5-[2-(2-pyridinyl)ethenyl]-3(2H)-furanoneHCID 5414433659.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-pyridinecarboxaldehyde (1.26 g, 10.2 mM) and 2,5-dimethyl-2-(4-fluorophenyl)-3(2H)-furanone (2.0 g, 9.8 mM) in ethanol (100 mL), was added 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 0.2 mL, 1.3 mM). The reaction solution was heated at 80° C. for 4 hours. After the reaction solution cooled to room temperature, saturated aqueous sodium chloride (400 mL) was added. The aqueous layer was extracted with diethyl ether (3×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give a yellow liquid. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to yield a yellow solid (1.7 g, 59% yield), m.p. 70°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010102
Source datasetuspto-grants-1991_04
ORD IDord-cb448e89e0e340eb8a57bdb2ac0915b4
Source noteuspto-grants-1991_04