Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051277Generated: October 27, 2026

Sodium Chloride → 2,2-Dimethyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/reaction/2051277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
Reactant3-ThiophenecarboxaldehydeHCID 68135—
Reactant3(2H)-Furanone, 2,2,5-trimethyl-HCID 137080—
SolventEthanolHCID 702—
Product2,2-Dimethyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanoneHCID 5434438380.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-thiophenecarboxaldehyde (1.5 g, 13.2 mM) and 2,2,5-trimethyl-3(2H)-furanone (1.5 g, 12 mM) in ethanol (100 mL), was added 1N aqueous sodium hydroxide (1.2 mL, 1.2 mM). The reaction solution was heated to 60° C. for 4 hours. After the reaction solution cooled, 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 crystalline solid. The residue was purified by chromatography (silica gel, hexane/ethyl acetate) to yield yellow crystals (2.1 g, 72% yield), m.p. 79°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017601
Source datasetuspto-grants-1991_05
ORD IDord-abaaf2d8948d4eedb814fdd99d7ef799
Source noteuspto-grants-1991_05