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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984316Generated: October 30, 2026

Sodium Carbonate → (E)-ethyl-3-(4'-chloro-biphenyl-4-yl)-but-2-enoate

https://huagongshe.com/reaction/984316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant(E)-ethyl 3-(4-bromophenyl)-but-2-enoateHCID 15933615—
SolventHydrochloric AcidHCID 313—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(E)-ethyl-3-(4'-chloro-biphenyl-4-yl)-but-2-enoateHCID 22557604—

Reaction Steps

Tetrakis(triphenylphoshine)palladium(0) (0.26 g, 0.22 mmol, 4 mol %) was added, under nitrogen, to a stirred solution of (E)-ethyl 3-(4-bromophenyl)-but-2-enoate (1.5 g, 5.57 mmol) {prepared as detailed in example 50 a} in DME (70 ml), and the resulting orange coloured solution stirred at room temperature for 10 min. Aqueous 2M sodium carbonate (16.7 ml, 33.4 mmol) was then added, the mixture stirred for 10 min, then 4-chlorophenyl boronic acid (1.3 g, 8.36 mmol) was added, and the reaction mixture heated to 80° C. for 18 h, under reflux. The reaction mixture was diluted with 1N HCl (100 ml) and the products extracted into ethyl acetate (2×100 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 (20% ethyl acetate in n-heptane eluent) to give the product, (E)-ethyl-3-(4′-chloro-biphenyl-4-yl)-but-2-enoate as a colourless solid; 1.17 g (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867218B2
Source datasetuspto-grants-2005_03
ORD IDord-e2e7ce1878b04af09efac478b6e6e93e
Source noteuspto-grants-2005_03