The synthetic method of diacyl peroxide
A technology of diacyl peroxide and synthesis method, which is applied in the preparation of peroxy compounds, chemical instruments and methods, preparation of organic compounds, etc., can solve the problems of expensive chemical raw materials and corrosion of acyl chloride, and achieves optimization of synthesis process and emission reduction. Effect
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Embodiment 1
[0058] In a 500ml three-necked bottle, add 200ml of petroleum ether (60-90°C), 28g of hydrogen peroxide with a purity of 27.5%, 72g of 3,5,5-trimethylhexanoic acid, and 6g of spherical polyvinyl alcohol compound amino acid A. The reaction mixture was stirred and heated to reflux temperature of 70-80°C. After azeotropic distillation, the distillate was cooled and the water of reaction was removed in a trap. The petroleum ether was separated off and returned to the reaction vessel. After reacting for 4 hours, gas chromatography analysis showed that the product yield of di-(3,5,5-trimethylhexanoyl) peroxide was 86.9%.
Embodiment 2
[0060] In a 500ml three-necked bottle, add 200ml of petroleum ether (60-90°C), 28g of hydrogen peroxide with a purity of 27.5%, 72g of 3,5,5-trimethylhexanoic acid, and 4g of spherical polyvinyl alcohol compound amino acid B. The reaction mixture was stirred and heated to reflux temperature of 70-80°C. After azeotropic distillation, the distillate was cooled and the water of reaction was removed in a trap. The petroleum ether was separated off and returned to the reaction vessel. After reacting for 4 hours, gas chromatography analysis showed that the product yield of di-(3,5,5-trimethylhexanoyl) peroxide was 65.6%.
Embodiment 3
[0062] In a 500ml three-necked bottle, add 200ml of petroleum ether (60-90°C), 28g of hydrogen peroxide with a purity of 27.5%, 72g of 3,5,5-trimethylhexanoic acid, and 2g of spherical polyvinyl alcohol compound amino acid C. The reaction mixture was stirred and heated to reflux temperature of 70-80°C. After azeotropic distillation, the distillate was cooled and the water of reaction was removed in a trap. The petroleum ether was separated off and returned to the reaction vessel. After reacting for 4 hours, gas chromatography analysis showed that the product yield of di-(3,5,5-trimethylhexanoyl) peroxide was 60.7%.
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