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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051264Generated: October 26, 2026

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

https://huagongshe.com/reaction/2051264

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 numberUS05017601
Source datasetuspto-grants-1991_05
ORD IDord-54678d439d5d4559914658f7ac6dfc4d
Source noteuspto-grants-1991_05