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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873393Generated: October 25, 2026

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

https://huagongshe.com/reaction/1873393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-IodoselenopheneHCID 142183—
ReactantB-(4-Ethoxy-2,3-difluorophenyl)boronic acidHCID 15135235—
Solventtert-Butyl methyl etherHCID 15413—
SolventToluene ethanolHCID 21863594—
Product2-(4-Ethoxy-2,3-difluorophenyl)selenopheneHCID 59456301—

Reaction Steps

A mixture of 34.8 g (0.14 mol) of 2-iodoselenophene, 32.8 g (0.16 mol) of 4-ethoxy-2,3-difluorophenylboronic acid, 8.10 g (77.01 mmol) of tetrakis -(triphenylphosphine)palladium(0) and 300 ml of 2 N sodium carbonate soln. in 800 ml of toluene/ethanol (1:1) is heated under reflux for 23 h. The mixture is diluted with MTBE and washed with water. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with 2 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:EtOAc=15:1-10:1→5:1). Further purification is carried out by recrystallisation from n-heptane; 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-0762230a08e74588a5910f25485ffb77
Source noteuspto-grants-2012_11