Application of Cyclotriveratrol and Its Derivatives in Olefin Polymerization Catalysts
A technology for olefin polymerization and derivatives is applied in the application field of cyclotriveratrol and its derivatives in olefin polymerization catalysts, and can solve the problems of poor versatility, ethyl benzoate cannot be used as a gas-phase polyethylene catalyst, and the like, to increase activity
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preparation example 1
[0129] Under ice-bath conditions, 1,2-phthalylene dimethyl ether (1.0g) was added dropwise to a mixture of aqueous formaldehyde (4mL / 38%) / 0.1mL chloroform / concentrated hydrochloric acid (6mL) for reaction, 30 After 1 min, the solution became a paste and stirring was continued for 4 h at room temperature. The solid was collected by filtration, washed with ice water, and thoroughly dried to obtain 0.5 g of compound A represented by formula (IV).
[0130]
preparation example 2
[0132] Under ice-bath conditions, 3-methoxy-4-bromo-benzyl alcohol (3.6 g) was dissolved in 30 mL of methanol, and 15 mL of 65% perchloric acid was added dropwise under ice-bath and stirring. Under nitrogen protection, the mixture was stirred in an ice bath for 18 h. 30 mL of water was slowly added to the reaction product, followed by extraction of the organic phase with dichloromethane. The organic phase was carefully washed with aqueous sodium hydroxide solution, then with deionized water, and dried. After exhausted and purified by column chromatography, 0.8 g of compound M represented by formula (V) was obtained.
[0133]
preparation example 3
[0135] Dissolve 1,2-o-phenylenediethyl ether (3.3g) and paraformaldehyde (0.63g) in dry dichloromethane (30mL), stir under ice bath, and slowly drop into boron trifluoride ether (4.25g) , after the dropwise addition, remove the ice-water bath, stir at room temperature for 3 h, follow the reaction by TLC until the reaction is complete, stop the reaction, wash the mixture 3 times with water, separate the organic layer, spin dry the organic solvent to obtain an oil, add a small amount of acetone to dissolve the oil The substance was dissolved, and a large amount of methanol was added to it, and it was left standing in the refrigerator to precipitate a white solid. After suction filtration and thorough drying, 1.5 g of compound B represented by formula (VI) was obtained.
[0136]
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