Catalyst used for coupling reaction of carbon dioxide and epoxy compound
A technology of epoxy compounds and carbon dioxide, which is applied in the direction of organic compound/hydride/coordination complex catalysts, physical/chemical process catalysts, catalyst activation/preparation, etc., can solve the difficulty of separating products from catalysts, high catalytic costs, and technical problems. Complicated and other issues, to achieve the effect of no heavy metal pollution, simple preparation steps, and low cost
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Embodiment 1
[0033] Embodiment 1: (ligand II 1 synthesis)
[0034] Take a 50mL three-necked flask, pump it three times under an argon atmosphere, and add 0.018mol 3-tert-butyl-5-(methylene-chloro(nitromethylimidazole)) salicylaldehyde (III 1 ), 30ml of ethanol was dissolved, 0.009mol cyclohexanediamine was added to the system, reacted at reflux temperature for 12 hours, stopped the reaction, cooled to room temperature, concentrated under a vacuum of 0.1MPa until the quality of the crude product was constant, and the concentrate was added with 15mL of ethyl acetate A light yellow precipitate appears, filter, collect the filter cake, and drain the filter cake under a vacuum of 0.1MPa to obtain Ligand II 1 , yield 82%.
Embodiment 2
[0035] Embodiment 2: (II 2 )
[0036] With 3-tert-butyl-5-(methylene-chloride (tri-n-butylamine)) salicylaldehyde (III 2) (0.018mol) instead of 3-tert-butyl-5-(methylene-chlorination (nitromethylimidazole)) salicylaldehyde (III 1 ), other operations are with embodiment 1, get II 2 , yield 73%.
Embodiment 3
[0037] Embodiment 3: (II 3 )
[0038] With 3-tert-butyl-5-(methylene-N-imidazole) salicylaldehyde (III 3 ) (0.018mol) instead of 3-tert-butyl-5-(methylene-chlorination (nitromethylimidazole)) salicylaldehyde (III 1 ), other operations are with embodiment 1, get II 3 , yield 80%.
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