Method of preparing arylamine chloride by high selective catalytic hydrogenation of chlorine substituent aromatic nitro compound
A technology for aromatic nitro and chlorinated aromatic amines, which is applied in the application field of catalytic hydrogenation to achieve the effects of simple production process and improved product purity
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Embodiment 1
[0012] Put 6g of p-chloronitrobenzene, 20mL of solvent, and 0.5g of Ru / C catalyst in a 70mL tank-type high-pressure reactor, seal it and replace the air, then fill it with 0.5MPa hydrogen, put it in an oil bath and heat it up slowly , adjust the hydrogen valve to make the system pressure reach 1MPa, and after 30 minutes, the reaction is complete. After cooling, samples are taken for capillary gas chromatography analysis, and the conversion rate of p-chloro-nitrobenzene is 100%, and the selectivity of p-chloroaniline is 100%.
Embodiment 2
[0014] Put 6g m-chloronitrobenzene, 20mL solvent, 0.5g Ru / C catalyst in a 70mL kettle-type high-pressure reactor, seal it and replace the air, then fill it with 0.5MPa hydrogen, put it in an oil bath and heat it up slowly , adjust the hydrogen valve to make the system pressure reach 1.5MPa, and after 30 minutes, the reaction is complete. After cooling, samples are taken for capillary gas chromatography analysis, the conversion rate of m-chloronitrobenzene is 100%, and the selectivity of m-chloroaniline is 100%.
Embodiment 3
[0016] Put 6g o-chloronitrobenzene, 20mL solvent, 0.5g Ru / C catalyst in a 70mL kettle-type high-pressure reactor, seal it and replace the air, then fill it with 0.5MPa hydrogen, put it in an oil bath and heat it up slowly , adjust the hydrogen valve to make the system pressure reach 1.5MPa, and after 30 minutes, the reaction is complete. After cooling, samples were taken for capillary gas chromatography analysis, and the conversion rate of o-chloronitrobenzene was 100%, and the selectivity of o-chloroaniline was 100%.
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