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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943513Generated: October 26, 2026

Sodium Carbonate → 2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-methylthiophene

https://huagongshe.com/reaction/1943513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-5-methylthiopheneHCID 69831—
Reactant4'-Ethyl-3-fluorobiphenyl-4-boronic acidHCID 53402575—
CatalystHCID 178418397HCID 178418397—
SolventToluene ethanolHCID 21863594—
Product2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-methylthiopheneHCID 58160695—

Reaction Steps

A mixture of 5.0 g (28.2 mmol) of 2-bromo-5-methylthiophene, 7.70 g (28.3 mmol) of 4′-ethyl-3-fluoro-4-biphenylboronic acid, 1.70 g (1.47 mmol) of tetrakis(triphenylphosphine)palladium(0) and 30 ml of 2 N sodium carbonate solution in 90 ml of toluene/ethanol (1:2) is refluxed for 3 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted a number of times with toluene. The combined organic phases are washed with water and sat. sodium chloride solution. The solution is dried using sodium sulfate and evaporated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:toluene=97:3). The further purification is carried out by recrystallisation from ethanol and n-heptane, giving 2-(4′-ethyl-3-fluorobiphenyl-4-yl)-5-methylthiophene as a colourless solid (m.p. 102° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394293B2
Source datasetuspto-grants-2013_03
ORD IDord-05f7bf8fa6664e07a70360f0b33c850a
Source noteuspto-grants-2013_03