Method for preparing 3-methyl-2-buten-1-ol through transesterification reaction of isopentenyl acetate
A technology for the transesterification of prenyl acetate and prenol, which is applied in the field of transesterification of prenyl acetate to prepare prenyl alcohol
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Embodiment 1
[0022] Embodiment 1 (comparative example)
[0023] The catalyst is CeO purchased from Sinopharm 2 , using a batch reactor, the catalytic reaction conditions are: 0.5g of prenyl acetate is mixed with 1.0mL of methanol, 50mg of catalyst is added, the reaction temperature is 140°C, the reaction pressure is 4Mpa, and the reaction time is 1.5h;
Embodiment 2
[0025] The catalyst is CeO 2 The carrier is loaded with precious metal Ir (Ir mass fraction is 2%). The specific preparation process is: impregnating the incipient wetness of a well-proportioned aqueous solution of chloroiridic acid onto the carrier for 24 hours, drying in an oven at 80°C for 12 hours, and drying in a muffle furnace. Calcined at 350°C for 2 hours to produce 2% Ir / CeO 2 solid acid catalyst. The prepared catalyst was reduced at 350° C. for 2 h under a hydrogen atmosphere. The reaction conditions are as follows: 0.5 g of prenyl acetate is mixed with 1.0 mL of methanol, 50 mg of catalyst is added, the reaction temperature is 140° C., the reaction pressure is 4 Mpa, and the reaction time is 1.5 h.
Embodiment 3
[0026] Embodiment 3 (comparative example)
[0027] Carrier CeO 2 Change to TiO 2 , other conditions are the same as in example 2.
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