Green preparation process for synthesizing 12-carbon alcohol ester by double catalytic system
A technology of dodecyl alcohol ester and catalyst is applied in the field of synthesis and preparation of fine chemical products to achieve the effects of simple production process, elimination of generation and elimination of waste water
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Embodiment 1
[0018] With 72g isobutyraldehyde, supported sodium hydroxide solid catalyst (carrier: montmorillonite, m(NaOH):m(montmorillonite)=0.7) 2.2g and hydroxide 1-butyl-3-methylimidazole 7.2g Add it into a 500mL four-neck flask equipped with a condenser heating device, heat to 60°C, stir for 4 hours, cool to room temperature, filter to separate the catalyst from the reaction system, analyze the reaction mixture, the conversion rate of isobutyraldehyde is 90%, select property of 94%, the unreacted isobutyraldehyde is removed by distillation under reduced pressure, and the product dodecyl alcohol ester with a content of more than 99.5% is continued to be collected.
Embodiment 2
[0020] 72g isobutyraldehyde, supported potassium hydroxide solid catalyst (carrier: activated carbon, m(KOH):m(activated carbon)=0.5), 1.5g and 1-butyl-3-methylimidazole hydroxide 10g were added to the equipped In the 500mL four-neck flask of the condenser heating device, heat to 50°C, stir for 3 hours, cool to room temperature, filter the catalyst to separate from the reaction system, and analyze the reaction mixture. The conversion rate of isobutyraldehyde is 95%, and the selectivity is 97%. Unreacted isobutyraldehyde is removed by distillation under reduced pressure, and the product dodecyl alcohol ester with a content of more than 99.5% is continued to be collected.
Embodiment 3
[0022] With 72g isobutyraldehyde, supported potassium carbonate solid catalyst (carrier: aluminum oxide, m (KCO 3 ): m (aluminum oxide) = 0.25), 3.6g and 8g of 1-methyl-3-methylimidazole hydroxide were added to a 500mL four-neck flask equipped with a condenser tube heating device, heated to 80°C, and stirred for 6h , cooled to room temperature, filtered to separate the catalyst from the reaction system, and analyzed the reaction mixture. The conversion rate of isobutyraldehyde was 88%, and the selectivity was 93%. Dodecyl alcohol esters.
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