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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943514Generated: November 2, 2026

Sodium Carbonate → HCID 58160694, compound

https://huagongshe.com/reaction/1943514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-BromothiopheneHCID 13851—
Reactant(3-Fluoro-4'-propyl[1,1'-biphenyl]-4-yl)boronic acidHCID 53402576—
CatalystHCID 178418397HCID 178418397—
SolventToluene ethanolHCID 21863594—
ProductHCID 58160694HCID 58160694—

Reaction Steps

A mixture of 25.3 g (0.16 mol) of 2-bromothiophene, 40.0 g (0.16 mol) of 4′-propyl-3-fluoro-4-biphenylboronic acid, 8.5 g (7.4 mmol) of tetrakis(triphenylphosphine)palladium(0) and 170 ml of 2 N sodium carbonate solution in 420 ml of toluene/ethanol (1:2) is refluxed for 18 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=9:1). The further purification is carried out by recrystallisation from ethanol and n-heptane, giving 2-(4′-propyl-3-fluorobiphenyl-4-yl)thiophene as a colourless solid (m.p. 88° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394293B2
Source datasetuspto-grants-2013_03
ORD IDord-b4374e14821b4f45b42b5d0526e9b7ca
Source noteuspto-grants-2013_03