HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943513Generated: October 26, 2026
Sodium Carbonate → 2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-methylthiophene
https://huagongshe.com/reaction/1943513
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromo-5-methylthiophene | HCID 69831 | — |
| Reactant | 4'-Ethyl-3-fluorobiphenyl-4-boronic acid | HCID 53402575 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | 2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-methylthiophene | HCID 58160695 | — |
Reaction Steps
A mixture of 5.0 g (28.2 mmol) of 2-bromo-5-methylthiophene, 7.70 g (28.3 mmol) of 4′-ethyl-3-fluoro-4-biphenylboronic acid, 1.70 g (1.47 mmol) of tetrakis(triphenylphosphine)palladium(0) and 30 ml of 2 N sodium carbonate solution in 90 ml of toluene/ethanol (1:2) is refluxed for 3 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:toluene=97:3). The further purification is carried out by recrystallisation from ethanol and n-heptane, giving 2-(4′-ethyl-3-fluorobiphenyl-4-yl)-5-methylthiophene as a colourless solid (m.p. 102° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394293B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-05f7bf8fa6664e07a70360f0b33c850a |
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| Source note | uspto-grants-2013_03 |
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