A method for catalytically synthesizing phenazine compounds under microwave irradiation in aqueous phase
A technology of microwave radiation and water phase, which is applied in the field of preparation of phenazine derivatives, can solve the problems of severe reaction conditions, difficulty in obtaining raw materials, and high toxicity of reagents, and achieves the effects of simple operation, environmental friendliness, and low cost
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Embodiment 1
[0042] Example 1: Phenazine: 1 mmol of 2-iodoaniline was added to the reaction vessel, followed by adding 0.1 mmol of ferric chloride, 0.1 mmol of lithium proline (proline lithiumas), 3 mmol of sodium hydroxide, 4-butyl bromide Ammonium (( n Bu) 4 NBr) 0.1 mmol, water 3 mL. Placed in a microwave reactor and heated to 100 °C under 150 W power for continuous reaction for 30 min. After the reaction was completed, it was cooled to room temperature, concentrated under reduced pressure, and the product was purified by column chromatography to obtain a yellow solid with a yield of 79%.
Embodiment 2
[0043] Example 2: 2,7-dimethylphenazine: 1 mmol of 2-iodo-4-methylaniline was added to the reaction vessel, followed by adding 0.1 mmol of ferric chloride and 0.1 mmol of lithium proline (proline lithiumas), Sodium hydroxide 3 mmol, 4-butylammonium bromide (( n Bu) 4 NBr) 0.1 mmol, water 3 mL. Placed in a microwave reactor and heated to 100 °C under 150 W power for 30 min. After the reaction was completed, it was cooled to room temperature, concentrated under reduced pressure, and the product was purified by column chromatography to obtain a yellow solid with a yield of 84%.
Embodiment 3
[0044] Example 3: 2,7-diethylphenazine: The preparation method is the same as in Example 2, adding 1 mmol of 2-iodo-4-ethylaniline to obtain a yellow solid with a yield of 86%.
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