Hindered amine light stabilizer and preparation method and application thereof
A technology of hindered amine light stabilizer and solvent is applied in the field of hindered amine light stabilizer and its preparation, and achieves the effects of good compatibility, high product yield, low volatility and low mobility
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Embodiment 1
[0048] The preparation of the compound shown in formula II:
[0049] Add 155g of triacetone amine, 81g of dimethylamine, 400g of xylene and 120g of formic acid in a 2L reactor, under the protection of nitrogen, start stirring and heat up to reflux state, after 6 hours, the sampling test is qualified, and the reaction solution Cool down to room temperature, wash with aqueous sodium hydroxide solution (30%, wt.) and deionized water to weak alkalinity, and distill under negative pressure to obtain an intermediate with a yield of 97.5%.
[0050] Put the obtained intermediate into a 2L reaction kettle, add 126g dimethyl malonate, 200g xylene and 10g ammonium lithium to the kettle, start stirring and raise the temperature to 130-135°C, after 4 hours, the sampling test is qualified , quenched with an organic acid after cooling, washed with water and dried, vacuum distillation to obtain the compound shown in the target product formula II (wherein, R is a methyl group, specifically sho...
Embodiment 2
[0054] A preparation method of a hindered amine light stabilizer, comprising the steps of:
[0055] In the reactor of 3L, add the compound shown in the gained formula II of 500g embodiment 1, 371g and 1-(2'-hydroxyethyl)-2,2,6,6-tetramethyl-4-piperidine Alcohol and 630mL xylene are under the protection of nitrogen, start stirring and preheat to 130-135°C, then add 18g of sodium methoxide, the reaction temperature rises to 170-175°C, and methanol is evaporated. After 9 hours, the sampling test is qualified, and the temperature is washed with water. , drying and decolorization, and vacuum distillation to obtain a white powder, which is the hindered amine light stabilizer shown in the following formula, and the product yield is 83.5%.
[0056]
[0057] Its molecular weight is between 2100 and 4200.
[0058] It can be seen from the infrared spectrum at 2980cm -1 、1465cm -1 、1380cm -1 absorption peak, indicating the presence of -CH 3 、-CH 2 - stretching, bending vibration vC...
Embodiment 3
[0060] In the reactor of 3L, add the compound shown in the gained formula II of 500g embodiment 1, 408g and 1-(2'-hydroxyethyl)-2,2,6,6-tetramethyl-4-piperidine Alcohol and 660mL xylene were under the protection of nitrogen, started to stir and preheated to 130-135°C, then added 4g of tetraethyl titanate, the reaction temperature was raised to 170-175°C, accompanied by the distillation of methanol, after 8 hours, the sampling test was qualified , washed with water at lower temperature, dried and decolorized, and vacuum distilled to obtain a light yellow powder with a product yield of 87.6% and a molecular weight between 2100 and 4200.
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