HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873434Generated: November 1, 2026
Sodium Carbonate → 2-(4'-Ethyl-2,3-difluorobiphenyl-4-yl)selenophene
https://huagongshe.com/reaction/1873434
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromoselenophene | HCID 137013 | — |
| Reactant | 2,3-Difluoro-4'-ethylbiphenyl-4-ylboronic acid | HCID 18469433 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | 2-(4'-Ethyl-2,3-difluorobiphenyl-4-yl)selenophene | HCID 59456295 | — |
Reaction Steps
A mixture of 56.0 g (0.27 mol) of 2-bromoselenophene, 70.0 g (0.27 mol) of 2,3-difluoro-4′-ethylbiphenyl-4-ylboronic acid, 22.0 g (19.0 mmol) of tetrakis(triphenylphosphine)palladium(0) and 800 ml of 2 N sodium carbonate soln. in 2.5 l of toluene/ethanol (1:1) is heated at 90° C. for 17 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted with toluene. The combined organic phases are washed with water, and the solution is dried using sodium sulfate. The solution is concentrated to dryness, and the residue is purified by column chromatography (SiO2, toluene). The further purification is carried out by recrystallisation from ethanol and n-heptane. 2-(4′-Ethyl-2,3-difluorobiphenyl-4-yl)-selenophene is obtained as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304036B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-8454be194d104d5eb45a02209f4523d5 |
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| Source note | uspto-grants-2012_11 |
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