Table 2.
RuCl3·3H2O-catalyzed reaction of indoles with aldehydes a.
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Entry | Compounds | R1 | R2 | Time/h | Yield [%] b |
1 | 2a | H | H | 0.5 | 92 |
2 | 2b | m-CH3 | H | 1 | 77 |
3 | 2c | p-CH3 | H | 1 | 83 |
4 | 2d | m-OCH3 | H | 1 | 81 |
5 | 2e | m-Cl | H | 0.5 | 93 |
6 | 2f | o-Br | H | 0.5 | 89 |
7 | 2g | m-NO2 | H | 0.5 | 98 |
8 | 3a | H | N-CH3 | 1 | 75 |
9 | 3b | m-CH3 | N-CH3 | 1 | 70 |
10 | 3c | p-CH3 | N-CH3 | 1 | 70 |
11 | 3d | m-OCH3 | N-CH3 | 1 | 73 |
12 | 3e | m-Cl | N-CH3 | 1 | 81 |
13 | 3f | o-Br | N-CH3 | 1 | 78 |
14 | 3g | m-NO2 | N-CH3 | 1 | 85 |
15 | 4a | m-CH3 | 2-CH3 | 0.5 | 80 |
16 | 4b | m-OCH3 | 2-CH3 | 0.5 | 78 |
a The reaction was performed with aldehyde (0.5 mmol), indole (1 mmol) and RuCl3·3H2O (0.05 mmol) in 1 mL of benzene at rt. b Isolated yield.