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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943520Generated: November 2, 2026

Sodium Bicarbonate → HCID 58028448, compound

https://huagongshe.com/reaction/1943520

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 refluxed 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 solution and dried using sodium sulfate. The solution is evaporated to dryness, 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 numberUS08394293B2
Source datasetuspto-grants-2013_03
ORD IDord-a745828eac674d2a92d6f02d31c3e488
Source noteuspto-grants-2013_03