HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298122Generated: October 30, 2026
(4-Fluoro-2-methylphenyl)boronic acid → 3-(4-Methylthiophenyl)-4-(2-methyl-4-fluorophenyl)thiophene
https://huagongshe.com/reaction/2298122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (4-Fluoro-2-methylphenyl)boronic acid | HCID 2734665 | — |
| Reactant | 3-(4-Methylsulfonylphenyl)-4-(4-fluorophenyl)thiophene | HCID 10426884 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 3-(4-Methylthiophenyl)-4-(2-methyl-4-fluorophenyl)thiophene | HCID 54562034 | 74.2% |
Reaction Steps
The mono-substituted thiophene from Example 14 (1.8 mmol, 520 mg) was combined with the 2-methyl-4-fluorophenyl boronic acid (2 eq, 3.6 mmol, 562 mg) in 8.0 ml of toluene, 4.3 ml of 2 M sodium carbonate, 10 ml of ethanol and tetrakis(triphenylphosphine)-palladium(0) (1.0 g) and was stirred at reflux overnight. The reaction was concentrated in vacuo and the residue was partitioned between toluene and water. The toluene layer was dried (MgSO4) and reconcentrated in vacuo. The residue was purified via silica chromatography (Waters, LC-2000) in 97% hexane/ethyl acetate to give 3-(4-methylthiophenyl)-4-(2-methyl-4-fluorophenyl)thiophene (420 mg) as a semi-solid, NMR (CDCl3) δ 1.90(s, 3H), 2.43(s, 3H), 6.8-6.9(m, 2H), 7.05(q, J=8 Hz, 4H), 7.12-7.18(m, 2H), 7.33(d, J=2 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492413B2 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-debf4b3ddf21493ca89c656688c09c20 |
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| Source note | uspto-grants-2002_12 |
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