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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873434Generated: November 1, 2026

Sodium Carbonate → 2-(4'-Ethyl-2,3-difluorobiphenyl-4-yl)selenophene

https://huagongshe.com/reaction/1873434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-BromoselenopheneHCID 137013—
Reactant2,3-Difluoro-4'-ethylbiphenyl-4-ylboronic acidHCID 18469433—
CatalystHCID 178418397HCID 178418397—
SolventToluene ethanolHCID 21863594—
Product2-(4'-Ethyl-2,3-difluorobiphenyl-4-yl)selenopheneHCID 59456295—

Reaction Steps

A mixture of 56.0 g (0.27 mol) of 2-bromoselenophene, 70.0 g (0.27 mol) of 2,3-difluoro-4′-ethylbiphenyl-4-ylboronic acid, 22.0 g (19.0 mmol) of tetrakis(triphenylphosphine)palladium(0) and 800 ml of 2 N sodium carbonate soln. in 2.5 l of toluene/ethanol (1:1) is heated at 90° C. for 17 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted with toluene. The combined organic phases are washed with water, and the solution is dried using sodium sulfate. The solution is concentrated to dryness, and the residue is purified by column chromatography (SiO2, toluene). The further purification is carried out by recrystallisation from ethanol and n-heptane. 2-(4′-Ethyl-2,3-difluorobiphenyl-4-yl)-selenophene is obtained as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-8454be194d104d5eb45a02209f4523d5
Source noteuspto-grants-2012_11