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. 2011 May 9;16(5):3855–3868. doi: 10.3390/molecules16053855

Table 2.

RuCl3·3H2O-catalyzed reaction of indoles with aldehydes a.

graphic file with name molecules-16-03855-i002.jpg
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.