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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085566Generated: October 25, 2026

Sodium Chloride → 5-[4-(4-Chlorophenyl)-1,3-butadienyl]-2,2-dimethyl-3(2H)-furanone

https://huagongshe.com/reaction/1085566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
Reactant3(2H)-Furanone, 2,2,5-trimethyl-HCID 137080—
Reactantp-ChlorocinnamaldehydeHCID 3794977—
SolventEthanolHCID 702—
Product5-[4-(4-Chlorophenyl)-1,3-butadienyl]-2,2-dimethyl-3(2H)-furanoneHCID 5422634242.7%

Reaction Steps

To a solution of p-chlorocinnamaldehyde (2.7 g, 16.2 mM) and 2,2,5-trimethyl-3(2H)-furanone (2.45 g, 19.4 mM) in ethanol (100 mL), was added 1N aqueous sodium hydroxide (32 mL, 3.2 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 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 brown solid. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to afford yellow crystals (1.9 g, 36% yield), m.p. 95°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010102
Source datasetuspto-grants-1991_04
ORD IDord-3829b95a9838451abb4eb1463c571c67
Source noteuspto-grants-1991_04