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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399410Generated: October 27, 2026

Phosphoric acid, disodium salt, dodecahydrate → 2-(3,5-Difluoro-4'-propylbiphenyl-4-yl)-5-propylthiophene

https://huagongshe.com/reaction/1399410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric acid, disodium salt, dodecahydrateHCID 61456—
Reactant2-Bromo-5-propylthiopheneHCID 21801904—
ReactantMonosodium phosphateHCID 23672064—
Reactant4'-Propyl-3,5-difluoro-4-biphenylboronic acidHCID 58028431—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(3,5-Difluoro-4'-propylbiphenyl-4-yl)-5-propylthiopheneHCID 58028428—

Reaction Steps

5.0 g (24.4 mmol) of 2-bromo-5-propylthiophene, 7.40 g (26.8 mmol) of 4′-propyl-3,5-difluoro-4-biphenylboronic acid and 2.82 g (2.44 mmol) of tetrakis(triphenylphosphine)palladium(0) are initially introduced in 160 ml of toluene. A solution of 5.85 g (48.8 mmol) of sodium dihydrogenphosphate and 13.8 g (97.5 mmol) of disodium hydrogenphosphate dodecahydrate in 50 ml of water is added, and the mixture is heated under reflux for 19 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). Further purification is carried out by recrystallisation from ethanol and n-heptane, giving 2-(3,5-difluoro-4′-propylbiphenyl-4-yl)-5-propylthiophene (PUS-3-3) as a colourless solid (m.p. 64° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906261B2
Source datasetuspto-grants-2014_12
ORD IDord-6abfc42a60b04f8f9a31f176251b538d
Source noteuspto-grants-2014_12