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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449734Generated: October 29, 2026

Sodium Bicarbonate → HCID 58028448, compound

https://huagongshe.com/reaction/449734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-2-fluoro-4'-pentyl-1,1'-biphenylHCID 22717515—
ReactantHCID 131730280HCID 131730280—
CatalystHCID 178418397HCID 178418397—
Solventtert-Butyl methyl etherHCID 15413—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 58028448HCID 58028448—

Reaction Steps

A mixture of 3.30 g (13.1 mmol) of 5-hexylthiophen-2-ylhydroxyboronic acid sodium salt, 4.20 g (13.1 mmol) of 4-bromo-2-fluoro-4′-pentylbiphenyl, 2.2 g (26.2 mmol) of sodium hydrogencarbonate and 0.70 g (0.61 mmol) of tetrakis(triphenylphosphine)palladium(0) in THF/water (1:1) is heated under reflux for 6 h. The mixture is diluted with MTBE, and the organic phase is separated off. The aqueous phase is extracted with MTBE. The combined organic phases are washed with sat. sodium chloride soln. and dried using sodium sulfate. The solution is concentrated to completion, and the residue is purified by column chromatography (SiO2, n-heptane). The further purification is carried out by recrystallisation from methanol/pentane (5:1). 2-(2-Fluoro-4′-pentylbiphenyl-4-yl)-5-hexylthiophene is obtained as a colourless solid having an m.p. of 44° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486297B2
Source datasetuspto-grants-2013_07
ORD IDord-0edbbba8d78547ea94b1f3eda102aa77
Source noteuspto-grants-2013_07