Method for preparing salicylic acid p-octyl phenyl ester as light stabilizer
A technology of octyl phenyl ester and light stabilizer, which is applied in the preparation field of light stabilizer p-octyl phenyl salicylate, can solve the problems of weak chlorination ability of thionyl chloride, low yield and the like, and achieves product yield. The effect of high rate, high product purity and short reaction time
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Embodiment 1
[0019] In a 250mL four-necked flask equipped with a thermometer, add 13.8g of salicylic acid, 7.4g of phosphorus oxychloride, 24.7g of p-octylphenol, and 38.7g of solvent, install a condenser tube, start the stirrer, and heat up to 90- At 110°C, stir slightly, and the reaction time is 5.5-9h. Under the condition of strong stirring, slowly pour the reactant into the solution of 15g anhydrous sodium carbonate in 450ml water, and separate and remove the excess phosphorus oxychloride and p-octyl base phenol. The solvent is recovered by vacuum distillation under reduced pressure, and the residue after removing the solvent is the crude product p-octylphenyl salicylate, and then recrystallized the crude product p-octylphenyl salicylate with absolute ethanol to obtain the product p-octylphenyl salicylate, product yield: 95.44%, melting point: 72-74°C.
Embodiment 2
[0021] In a 250mL four-necked flask equipped with a thermometer, add 13.8g of salicylic acid, 7.4g of phosphorus oxychloride, 25.7g of p-octylphenol, and 33g of solvent, install a condenser, start the agitator, and heat up to 90-110 ℃, stir slightly, and the reaction time is 5.5-9h. Under the condition of strong stirring, slowly pour the reactant into the solution of 15g of anhydrous sodium carbonate in 450ml of water, and separate and remove the excess phosphorus oxychloride and p-octyl phenol. The solvent is recovered by vacuum distillation under reduced pressure, and the residue after removing the solvent is the crude product p-octylphenyl salicylate, and then recrystallized the crude product p-octylphenyl salicylate with absolute ethanol to obtain the product p-octylphenyl salicylate, product yield: 95.82%, melting point: 72-74°C.
Embodiment 3
[0023] In a 250mL four-neck flask equipped with a thermometer, add 13.8g of salicylic acid, 7.4g of phosphorus oxychloride, 26.8g of p-octylphenol, and 40g of solvent, install a condenser tube, start the stirrer, and heat up to 90-110 ℃, stir slightly, and the reaction time is 5.5-9h. Under the condition of strong stirring, slowly pour the reactant into the solution of 15g of anhydrous sodium carbonate in 450ml of water, and separate and remove the excess phosphorus oxychloride and p-octyl phenol. The solvent is recovered by vacuum distillation under reduced pressure, and the residue after removing the solvent is the crude product p-octylphenyl salicylate, and then recrystallized the crude product p-octylphenyl salicylate with absolute ethanol to obtain the product p-octylphenyl salicylate, product yield: 95.91%, melting point: 72-74°C.
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