Preparation method of N-methyl-p-anisidine
A technology of p-methoxyaniline and methyl, which is applied in the field of preparation of N-methyl-p-methoxyaniline (NMPA), can solve problems such as high-pressure hydrogen, achieve less by-products, economical and easy atom utilization, and Equipment requires simple effects
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Embodiment 1
[0022] Weigh 1 mmol of copper nitrate trihydrate, 10 mmol of nickel nitrate hexahydrate, and 5 mmol of zinc nitrate hexahydrate into 100 mL of deionized water, stir and dissolve in a 250 mL round bottom flask, add 50 mL of 0.4 M sodium carbonate solution dropwise Stir well into the above solution, 50 o C aged for 3 h, centrifuged and washed with deionized water until neutral, and the precipitate was 100 o C drying 3 h, muffle furnace 400 o C roasting for 2 h, using a temperature-programmed reduction furnace, at a hydrogen flow rate of 10 mL / min, 10 o C / min heating up to 450 o C, at 450 o C for 2 h to obtain prefabricated catalyst A1.
Embodiment 2
[0024] Weigh 3 mmol of copper nitrate trihydrate, 6 mmol of nickel nitrate hexahydrate, and 10 mmol of zinc nitrate hexahydrate into 100 mL of deionized water, stir and dissolve in a 250 mL round bottom flask, add 60 mL of 1 M ammonia solution dropwise to the above Stir well in the solution, 50 o C aged for 3 h, centrifuged and washed with deionized water until neutral, and the precipitate was 100 o C drying 3 h, muffle furnace 400 o C roasting for 2h, using a temperature-programmed reduction furnace, at a hydrogen flow rate of 10 mL / min, 10 o C / min heating up to 450 o C, at 450 o C for 2 h to obtain prefabricated catalyst A2.
Embodiment 3
[0026]Weigh 10 mmol of copper nitrate trihydrate, 2 mmol of nickel nitrate hexahydrate, and 2 mmol of zinc nitrate hexahydrate into 100 mL of deionized water, stir and dissolve in a 250 mL round bottom flask, and add 45 mL of 0.8 M sodium hydroxide solution dropwise to the above solution Stir well in medium, 50 o C aged for 3h, centrifuged and washed with deionized water until neutral, and the precipitate was 100 o C drying 3 h, muffle furnace 400 o C roasting for 2 hours, using a temperature-programmed reduction furnace, at a hydrogen flow rate of 10 mL / min, 10 o C / min heating up to 450 o C, at 450 o C for 2 h to obtain prefabricated catalyst A3.
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