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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449738Generated: October 30, 2026

Toluene → HCID 58028435, compound

https://huagongshe.com/reaction/449738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTolylboronic acidHCID 79799—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58028434HCID 58028434—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventToluene ethanolHCID 21863594—
ProductHCID 58028435HCID 58028435—

Reaction Steps

A mixture of 3.54 g (26.0 mmol) of p-tolylboronic acid, 8.50 g (26.0 mmol) of 2-bromo-5-(3-fluoro-4-pentylphenyl)thiophene, 1.50 g (1.30 mmol) of tetrakis(triphenylphosphine)palladium(0) and 33 ml of 2 M sodium hydrogencarbonate soln. in 80 ml of ethanol/toluene=3:2 is heated at 80° C. for 20 h. Toluene and water are added to the mixture, and the organic phase is separated off. The aqueous phase is extracted with toluene, and the combined organic phases are washed with sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to completion. The residue is purified by column chromatography (SiO2, toluene). The further purification is carried out by recrystallisation from ethanol and n-heptane. 2-(3-Fluoro-4-pentylphenyl)-5-p-tolylthiophene is obtained as a solid having an m.p. of 115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486297B2
Source datasetuspto-grants-2013_07
ORD IDord-1e4c746ea26247a9bd5a90d72df3bf39
Source noteuspto-grants-2013_07