Catalyst used for synthesis of p-tolualdehyde
A technology of p-tolualdehyde and catalyst, applied in organic compound/hydride/coordination complex catalyst, physical/chemical process catalyst, organic chemistry, etc., can solve the problem of low selectivity of tolualdehyde
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Embodiment 1
[0040] Catalyst preparation: under nitrogen atmosphere, AlCl 3 (40.0 g, 0.3 mol) was slowly added to N,N-dimethyl imidazole chloride (26.2 g, 0.15 mol), stirred and reacted at 40° C. for 4 h to obtain the catalyst. Elemental analysis: theoretically calculated value C, 15.04; H, 2.27; N, 7.02. Experimental values C, 15.07; H, 2.28; N, 7.01.
[0041] Carbonylation reaction: Add the above catalyst (79.9g, 0.2mol) and toluene (9.2g, 0.1mol) into a 250ml autoclave; replace the air in the kettle with CO gas; raise the temperature to 50°C, keep the reaction pressure at 4.0MPa, and stir at 800rpm , Reacted for 5h to obtain a product mixture containing p-tolualdehyde.
[0042] For the convenience of comparison and illustration, the composition parameters in the catalyst active components and the corresponding selectivity to p-tolualdehyde are listed in Table 1.
Embodiment 2
[0044] Catalyst preparation: under nitrogen atmosphere, RuCl3 (62.2g, 0.3mol) was slowly added into N,N-dimethyl imidazole chloride (26.2g, 0.15mol), stirred and reacted at 40°C for 4h to obtain the catalyst. Elemental analysis: theoretically calculated value C, 10.97; H, 1.66; N, 5.12. Experimental values C, 10.95; H, 1.65; N, 5.13.
[0045] Carbonylation reaction: Add the above catalyst (109.5g, 0.2mol) and toluene (9.2g, 0.1mol) into a 250ml autoclave; replace the air in the kettle with CO gas; raise the temperature to 50°C, keep the reaction pressure at 4.0MPa, and stir at 800rpm , Reacted for 5h to obtain a product mixture containing p-tolualdehyde.
[0046] For the convenience of comparison and illustration, the composition parameters in the catalyst active components and the corresponding selectivity to p-tolualdehyde are listed in Table 1.
Embodiment 3
[0048] Catalyst preparation: under nitrogen atmosphere, PdCl 2 (53.2g, 0.3mol) was slowly added into N,N-dimethyl imidazole chloride (26.2g, 0.15mol), stirred and reacted at 40°C for 4h to obtain the catalyst. Elemental analysis: theoretically calculated value C, 12.33; H, 1.86; N, 5.75. Experimental values C, 12.29; H, 1.86; N, 5.77.
[0049] Carbonylation reaction: Add the above catalyst (97.5g, 0.2mol) and toluene (9.2g, 0.1mol) into a 250ml autoclave; replace the air in the kettle with CO gas; raise the temperature to 50°C, keep the reaction pressure at 4.0MPa, and stir at 800rpm , Reacted for 5h to obtain a product mixture containing p-tolualdehyde.
[0050] For the convenience of comparison and illustration, the composition parameters in the catalyst active components and the corresponding selectivity to p-tolualdehyde are listed in Table 1.
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