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. 2010 Aug 27;15(9):5909–5927. doi: 10.3390/molecules15095909

Table 3.

Friedel−Crafts type cyclization of benzofurans 20

graphic file with name molecules-15-05909-i003.jpg
Entry R R1 Ar2 20 Yield (%) a
1(a) A 3,5-(MeO)2 C6H5 95
2(b) A 3,5-(MeO)2 4-(MeO)C6H4 90
3(c) A 3,5-(MeO)2 2-furyl 0
4(d) A H 4-(MeO)C6H4 0
5(e) A 3,4,5-(MeO)3 4-(MeO)C6H4 92
6(f) A 3,4-(MeO)2 4-(MeO)C6H4 90
7(g) B 3,4-(MeO)2 4-(MeO)C6H4 95

Reagents and conditions: (a) p-TsOH•H2O (3.0 equiv), CH2Cl2, 40 °C, 8 h. aYields refer to chromatographically and spectroscopically homogeneous material.