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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984352Generated: October 29, 2026

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

https://huagongshe.com/reaction/984352

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 numberUS06867218B2
Source datasetuspto-grants-2005_03
ORD IDord-5a9380a62c5e4891b429ae0f74105b64
Source noteuspto-grants-2005_03