反应详情

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).

1. temperatureat reflux overnight
2. concentrationThe reaction was concentrated in vacuo
3. customthe residue was partitioned between toluene and water
4. dry with materialThe toluene layer was dried (MgSO4)
5. customThe residue was purified via silica chromatography (Waters, LC-2000) in 97% hexane/ethyl acetate