Light stabilizer and production method thereof
A light stabilizer and production method technology, applied in the direction of organic chemistry, can solve the problems of large pollution, poor product quality, and easy-to-corrosion equipment, and achieve the effects of simplifying the separation and purification process, short reaction time, and small environmental pollution
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Embodiment 1
[0019] In a 250mL four-neck flask equipped with a thermometer, add xylene 40g, dimethyl sebacate 23.0g (0.1mol), 1,2,2,6,6-pentamethyl-4-hydroxypiperidine 28.26 g (0.165mol), catalyzer 1g, this catalyzer is dibutyl tin oxide, loads on condenser, starts agitator, when being warmed up to 110-130 ℃, constantly steams the methyl alcohol that generates in the reaction process, reaction time 2.5h ( The reaction was monitored by liquid chromatography). After the reaction is finished, filter and wash with water, collect the organic phase, and dewater, decolorize, and desolventize the organic phase to obtain the light stabilizer-292 with a product yield of 96.31%.
Embodiment 2
[0021] In a 250mL four-neck flask equipped with a thermometer, add xylene 40g, dimethyl sebacate 23.0g (0.1mol), 1,2,2,6,6-pentamethyl-4-hydroxypiperidine 28.26 g (0.165mol), catalyst 1.2g, the catalyst is dibutyltin oxide, install a condenser, start the agitator, when the temperature rises to 110-130°C, the methanol generated during the reaction is continuously distilled out, and the reaction time is 2.5h (Reaction monitored by liquid chromatography). After the reaction is finished, filter and wash with water, collect the organic phase, and dewater, decolorize, and desolventize the organic phase to obtain Light Stabilizer-292 with a product yield of 96.67%.
Embodiment 3
[0023] In a 250mL four-neck flask equipped with a thermometer, add xylene 40g, dimethyl sebacate 23.0g (0.1mol), 1,2,2,6,6-pentamethyl-4-hydroxypiperidine 29.12 g (0.17mol), catalyst 1.0g, the catalyst is dibutyltin oxide, install a condenser, start the agitator, when the temperature rises to 110-130°C, the methanol generated during the reaction is continuously distilled out, and the reaction time is 2.5h (Reaction monitored by liquid chromatography). After the reaction is finished, filter and wash with water, collect the organic phase, and dewater, decolorize, and desolventize the organic phase to obtain the light stabilizer-292 with a product yield of 96.84%.
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