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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphoric acid, disodium salt, dodecahydrate | HCID 61456 | — |
| Reactant | 2-Bromo-5-propylthiophene | HCID 21801904 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | 4'-Propyl-3,5-difluoro-4-biphenylboronic acid | HCID 58028431 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(3,5-Difluoro-4'-propylbiphenyl-4-yl)-5-propylthiophene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906261B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-6abfc42a60b04f8f9a31f176251b538d |
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| Source note | uspto-grants-2014_12 |
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