Method for catalytically synthesizing phenazine compounds in water phase under microwave radiation
A technology of microwave irradiation and aqueous phase, applied in the direction of organic chemistry, can solve the problems of difficulty in obtaining raw materials, severe reaction conditions, and high toxicity of reagents, and achieve the effects of environmental friendliness, simple operation and low cost.
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Embodiment 1
[0042] Example 1: Phenazine: Add 1mmol of 2-iodoaniline to the reaction vessel, add 0.1mmol of iron chloride, 0.1mmol of lithium proline (prolinelithiumas), 3mmol of sodium hydroxide, and 4-butylammonium bromide (( n Bu) 4 NBr) 0.1mmol, water 3mL. Placed in a microwave reactor and heated to 100°C under 150W power for continuous reaction for 30min. After the reaction, it was cooled to room temperature and concentrated under reduced pressure. 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: Add 1mmol of 2-iodo-4-methylaniline to the reaction vessel, add 0.1mmol of ferric chloride, 0.1mmol of lithium proline (prolinelithiumas), 3mmol of sodium hydroxide, and 4-butylammonium bromide (( n Bu) 4 NBr) 0.1mmol, water 3mL. Placed in a microwave reactor and heated to 100°C under 150W power for continuous reaction for 30min. After the reaction, it was cooled to room temperature and concentrated under reduced pressure. 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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