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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943522Generated: November 1, 2026

Toluene → HCID 58028440, compound

https://huagongshe.com/reaction/1943522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Thiopheneboronic acidHCID 2733960—
ReactantHCID 22717522HCID 22717522—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventToluene ethanolHCID 21863594—
ProductHCID 58028440HCID 58028440—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 40.0 g (0.31 mol) of thiophen-2-ylboronic acid, 80.0 g (0.32 mol) of 4-bromo-2-fluoro-1-pentylbenzene, 18.0 g (15.6 mmol) of tetrakis(triphenylphosphine)palladium(0) and 400 ml of 2 M sodium hydrogencarbonate solution in 1000 ml of ethanol/toluene=3:2 is heated at 80° C. for 19 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 solution. The solution is dried using sodium sulfate and evaporated to dryness. The residue is purified by column chromatography (SiO2, n-heptane). 2-(3-Fluoro-4-pentylphenyl)thiophene is obtained as a colourless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394293B2
Source datasetuspto-grants-2013_03
ORD IDord-3b1e28fd45264062b4e403d03c823688
Source noteuspto-grants-2013_03