Preparation method of methanamide
A formamide and secondary amine technology, applied in the field of formamide preparation, can solve the problems of environmental pollution, complex catalyst preparation process, and low reaction yield
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Embodiment 1
[0028] CeO obtained by roasting method 2 The process is as follows: directly roast cerium ammonium nitrate at 650°C for 2 hours, and the obtained CeO 2 , denoted as CEO-1, applied to the reaction of benzylamine with N,N-dimethylformamide. In a 150ml Teflon-lined reactor, add 15mmol benzylamine and 20ml N,N-dimethylformamide respectively, weigh 1g CEO-1 to catalyze the reaction, stir the reaction at 100°C for 12h, after the reaction , the chromatographic detection product, its conversion rate and selectivity are shown in Table 1.
Embodiment 2
[0030] CeO obtained by co-precipitation method 2 The process is as follows: dissolve cerium nitrate in water, adjust the pH to 11 with ammonia water, filter and separate, dry the filter cake at 100°C overnight, and roast at 500°C for 4 hours to obtain CeO 2 Denoted as CEO-2, it is used in the hydrolysis reaction of benzylamine and N,N-dimethylformamide. In a 150ml Teflon-lined reactor, add 15mmol benzylamine and 20ml N,N-dimethylformamide respectively, weigh 1g CEO-2 to catalyze the reaction, stir the reaction at 100°C for 12h, after the reaction , the chromatographic detection product, its conversion rate and selectivity are shown in Table 1.
Embodiment 3
[0032] Dissolve cerium ammonium nitrate and polyvinylpyrrolidone in ethylene glycol, reflux at 190°C for 24 hours, filter and separate, vacuum-dry the filter cake at 80°C, and roast at 600°C to obtain CeO 2 Denoted as CEO-3, it is used in the hydrolysis reaction of benzylamine and N,N-dimethylformamide. In a 150ml Teflon-lined reactor, add 15mmol benzylamine and 20ml N,N-dimethylformamide respectively, weigh 1g CEO-3 to catalyze the reaction, stir the reaction at 100°C for 12h, after the reaction , the chromatographic detection product, its conversion rate and selectivity are shown in Table 1.
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