Double indolyl derivative synthesizing process
A technology of indole alkyl and synthesis method, which is applied in the field of preparation of heterocyclic compounds, can solve problems such as not seen, and achieve the effects of no reduction in activity, avoiding pollution, and simple operation
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Embodiment 1
[0016] Embodiment one: the synthesis of bis-indolylmethane
[0017] Take 1 mmol of formaldehyde and 2 mmol of indole in a grinder, add solid super acid SO 4 2- / TiO 2 Catalyst, the dosage is 50 mg, ground and reacted at 50°C for 0.5-1.5 hours, then washed with ethyl acetate, filtered, and the filtrate is concentrated to obtain a crude product, which is further purified to obtain bis-indolylmethane with higher purity.
Embodiment 2
[0018] Embodiment two: the synthesis of bisindolephenyl methane
[0019] Take 1 mmol of benzaldehyde and 2 mmol of indole in a reaction flask, add 60 mg of solid superacid SO 4 2- / TiO 2 , placed in a grinder, ground evenly, heated up to about 50°C under an infrared lamp, after 0.5 hours, TLC detected that the reaction was complete, washed with ethyl acetate, filtered, and the filtrate was concentrated in vacuum to obtain a crude product, which was further purified to obtain a higher Purity bisindolephenylmethane.
[0020]
Embodiment 3
[0021] Embodiment three: the synthesis of bis-indoxythiophene methane
[0022] Take 1 mmol of thiophene-2-carbaldehyde and 2 mmol of indole in a reaction flask, add 45 mg of solid superacid SO 4 2- / TiO 2 , placed in a grinder, ground evenly, heated to about 50°C under an infrared lamp, after 1.5 hours, TLC detected that the reaction was complete, washed with ethyl acetate, filtered, and the filtrate was concentrated in vacuum to obtain a crude product, which was further purified to obtain a higher Purity bisindolephenylmethane.
[0023]
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