Hydrolysis method of esters
A kind of ester, said technology, applied in the field of ester hydrolysis, can solve the problems of high price, high cost of industrial use, loss of activity, etc., and achieve the effect of cheap price, low cost and easy separation
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Embodiment 1
[0024] Weigh 20g of phosphotungstic acid dried at 100°C and dissolve it in 80g of pure water to make solution A; weigh 0.67g of ammonium carbonate and dissolve it in 6g of water to make solution B; B. Stir fully; continue stirring for 40 minutes after the dropwise addition is completed; dry at 80°C to obtain the following catalyst: NH 4 h 2 PW 12 o 40 .
[0025] 10.00 g of the catalyst, 67.25 g of methyl acetate, and 32.75 g of water were charged into a 250 ml batch reactor, and the temperature was raised to 100° C. to hydrolyze the methyl acetate for 90 minutes. When the reaction product was collected and analyzed, the conversion rate of methyl acetate was 47.8%.
Embodiment 2
[0027] Weigh 5g of phosphotungstic acid dried at 100°C and dissolve it in 20g of water to make solution A; weigh 0.10g of ethylenediamine and dissolve it in 2g of methanol to make solution B; add the solution to solution A dropwise B. Stir fully; continue stirring for 40 minutes after the dropwise addition is completed; dry at 80°C to obtain the following catalyst: NH 4 CH 2 CH 2 NHH 2 PW 12 o 40 .
[0028] 10.00 g of the catalyst, 74.00 g of methyl butyrate, and 26.10 g of water were charged into a 250 ml three-necked bottle. The temperature was raised to 80° C. to hydrolyze methyl butyrate, and the reaction was carried out for 150 minutes. When the reaction product was collected and analyzed, the conversion rate of methyl butyrate was 24.4%.
Embodiment 3
[0030] Weigh 20g of silicotungstic acid dried at 100°C and dissolve it in 80g of pure water to make solution A; weigh 0.56g of ammonium nitrate and dissolve it in 5g of water to make solution B; add solution to solution A B, fully stir; continue to stir for 40 minutes after the dropwise addition is completed; add an appropriate amount of silicon dioxide fine powder to the mixture, and continue to stir vigorously for 60 minutes; dry and calcinate to obtain the following catalyst: NH 4 h 3 SiW 12 o 40 / SiO 2 .
[0031] 10.00 g of the catalyst, 81.00 g of ethyl benzoate, and 19.30 g of water were charged into a 250 ml batch reactor. The temperature was raised to 100° C., and ethyl benzoate was hydrolyzed for 120 minutes. When the reaction product was collected and analyzed, the conversion rate of ethyl benzoate was 44.8%.
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