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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873394Generated: October 25, 2026

Sodium Carbonate → 2-(4-Ethoxy-2,3-difluorophenyl)selenophene

https://huagongshe.com/reaction/1873394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-BromoselenopheneHCID 137013—
ReactantB-(4-Ethoxy-2,3-difluorophenyl)boronic acidHCID 15135235—
CatalystHCID 178418397HCID 178418397—
SolventToluene ethanolHCID 21863594—
Product2-(4-Ethoxy-2,3-difluorophenyl)selenopheneHCID 59456301—

Reaction Steps

A mixture of 45.0 g (0.21 mol) of 2-bromoselenophene, 52.0 g (0.26 mol) of 4-ethoxy-2,3-difluorophenylboronic acid, 20.0 g (17.3 mmol) of tetrakis(triphenylphosphine)palladium(0) and 600 ml of 2 N sodium carbonate soln. in 1100 ml of toluene/ethanol (1:1) is heated under reflux for 20 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted with toluene. The combined organic phases are washed with sat. sodium hydrogencarbonate soln., 1 N hydrochloric acid and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:toluene=3:2). Further purification is carried out by recrystallisation from ethanol; 2-(4-ethoxy-2,3-difluorophenyl)selenophene is obtained as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-b0d75b2282834822b4ffc49a3ff86c7a
Source noteuspto-grants-2012_11