Ester compound and application thereof in catalyst for olefin polymerization
An ester compound, selected technology, applied in the direction of organic chemistry, etc., can solve the problems of low catalytic activity and narrow molecular mass distribution of polymers
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Embodiment 1~3
[0047] Embodiment 1~3 prepares 1-acyloxy-3-alkoxypropane compounds
Embodiment 1
[0048] Example 1: Preparation of 2,2-dimethyl-1-o-toluoyloxy-3-methoxypropane
[0049] Add 1.6 g of 2,2-dimethyl-3-methoxy-1-propanol into a 100 ml three-neck flask, and then add 20 ml of dichloromethane. Stir and add 1.5 ml pyridine. Add 10ml of dichloromethane to the constant pressure dropping funnel, and dissolve 2.5ml of o-toluoyl chloride in it. Under stirring conditions, o-benzoyl chloride solution was added dropwise. React at room temperature for 12 hours. After stopping the reaction, add 30 ml of 5% hydrochloric acid solution to wash twice, then wash with 30 ml of saturated sodium bicarbonate solution for 2 to 3 times, and finally wash with water until the pH value is 7. The organic layer was separated and dried overnight by adding anhydrous magnesium sulfate. Filter and evaporate the solvent dichloromethane. The obtained crude product was separated and purified by column chromatography. The filler is 60-80 mesh silica gel for column chromatography, and the eluen...
Embodiment 2
[0052] Example 2: Preparation of 2,2-dimethyl-1-m-toluoyloxy-3-methoxypropane
[0053] According to the operation method of Example 2, 5.1g of 2,2-dimethyl-3-methoxyl-1-propanol, 3.6ml of pyridine, and 6ml of m-toluoyl chloride undergo an acylation reaction, and the obtained crude product is purified by distillation under reduced pressure , to give 2,2-dimethyl-1-m-toluoyloxy-3-methoxypropane.
[0054] Elemental analysis: C content: 71.43%; H content: 8.35%. (the compound C 14 h 20 o 3 Theoretical content of elements: C, 71.16%; H, 8.53%).
[0055] 1 H-NMR (300MHZ, CDCl 3 )(δ, ppm): 1.03(s, 6H, C(CH 3 ) 2 ), 2.41(s, 3H, ArCH 3 ), 3.24(s, 2H, CH 2 OCH 3 ), 3.34(s, 3H, OCH 3 ), 4.13 (s, 2H, COOCH 2 ), 7.26-7.35 (t, 2H, ArH), 7.83-7.85 (d, 2H, ArH).
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