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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268294Generated: October 31, 2026

Sodium Carbonate → (E)-ethyl 3-(4-furan-2-yl-phenyl)-but-2-enoate

https://huagongshe.com/reaction/1268294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantFuran-2-boronic acidHCID 2734357—
Reactant(E)-ethyl 3-(4-iodophenyl)-but-2-enoateHCID 11438459—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(E)-ethyl 3-(4-furan-2-yl-phenyl)-but-2-enoateHCID 22557549—

Reaction Steps

Tetrakis(triphenylphoshine)palladium(0) (0.69 g, 0.60 mmol, 6 mol %) was added, under nitrogen, to a stirred solution of (E)-ethyl 3-(4-iodophenyl)-but-2-enoate (3.16 g, 10.0 mmol) in DME (100 ml), and the resulting orange coloured solution stirred at room temperature for 10 min. Aqueous 2M sodium carbonate (30.0 ml, 60.0 mmol) was then added, the mixture stirred for 10 min, then furan-2-boronic acid (2.25 g, 20.11 mmol) was added, and the reaction mixture heated to 80° C. for 20 h, under reflux. The reaction mixture was cooled, diluted with water (100 ml) and the products extracted into ethyl acetate (3×100 ml). The combined organic extracts were washed with brine, dried (MgSO4), and evaporated to give the crude product, which was purified by column chromatography on silica gel (3% diethyl ether in n-heptane eluent) to give the product, (E)-ethyl 3-(4-furan-2-yl-phenyl)-but-2-enoate as an off-white solid; 2.46 g (96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555577B1
Source datasetuspto-grants-2003_04
ORD IDord-d68edd57549443d3ad1ac31f373985d6
Source noteuspto-grants-2003_04