Cationic polymerization method
A cationic polymerization and carbocation technology, which is applied in the field of cationic polymerization, can solve the problems of difficult and unsatisfactory initiator system preparation, high technical requirements for the preparation of aluminoxane, etc., and achieve reduced energy consumption, improved initiation efficiency, and high Effect of Polymer Yield
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preparation example 1
[0085] Preparation Example 1: Synthesis of 2-chloro-2,4,4-trimethylpentane (TMPCl)
[0086] Place a 250mL three-necked round-bottom flask in an ice-water bath, and then add 30mL of 2,4,4-trimethyl-1-pentene and 30mL of dichloromethane. Under the condition of continuously feeding dry hydrogen chloride gas, the reaction was carried out for 5h. The mixture obtained by the reaction was neutralized with sodium bicarbonate, then anhydrous magnesium sulfate was added to the solution, and then filtered, the liquid mixture was collected, and vacuum distillation was carried out to collect the fraction at 44°C (2.1332kPa) (yield: 70 % by weight, its purity was determined to be 93% by gas chromatography analysis). After characterization, it was confirmed that the fraction was 2-chloro-2,4,4-trimethylpentane. in, 1 H-NMR (δ, ppm): 1.06(-C(CH 3 ) 3 ), 1.67(-C(CH 3 ) 2 Cl), 1.88(-CH 2 -).
preparation example 2
[0087] Preparation Example 2: Synthesis of Dicumyl Chloride
[0088] Put a 500mL three-necked round-bottomed cauldron equipped with bottomed inlet and outlet pipes and a magnetic stirring device in an ice-water bath, and then add 8g of p-dicumyl alcohol and 10g of CaCl 2 and 100 g of dichloromethane. Continuously feed dry hydrogen chloride gas into the three-necked flask, and stir and react for 10 hours. After the reaction was completed, it was filtered to obtain a clear solution. Hydrogen chloride and methylene chloride were removed in vacuo to obtain 9.1 g of colorless needle crystals (yield: 96% by weight). Dissolve the obtained needle-shaped crystals in 50 mL of n-hexane, filter to remove insoluble impurities, cool the remaining liquid phase to -20°C to -30°C, crystallize with stirring, separate the precipitated crystals from the mother liquor, and collect the crystals. The crystal was determined to be p-dicumyl chloride through characterization. in, 1 H-NMR (δ, ppm): ...
preparation example 3
[0089] Preparation Example 3: Synthesis of p-dicumyl bromide
[0090] p-Dicumyl bromide was prepared in a method similar to Preparation Example 2, except that hydrogen chloride gas was replaced by hydrogen bromide gas. in, 1 H-NMR (δ, ppm): 2.11 ( ), 7.06 (phenyl).
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