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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Fluoro-2-methylphenyl)boronic acidHCID 2734665—
Reactant3-(4-Methylsulfonylphenyl)-4-(4-fluorophenyl)thiopheneHCID 10426884—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventSodium CarbonateHCID 10340—
Product3-(4-Methylthiophenyl)-4-(2-methyl-4-fluorophenyl)thiopheneHCID 5456203474.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492413B2
Source datasetuspto-grants-2002_12
ORD IDord-debf4b3ddf21493ca89c656688c09c20
Source noteuspto-grants-2002_12