Method of preparing isopulegol by cyclization reaction of citronellal
A technology of isopulegol and cyclization reaction, which is applied in the fields of chemical instruments and methods, reduction preparation of oxygen-containing functional groups, organic chemistry, etc., can solve the problems of unsuitable large-scale industrial production, frequent catalyst recycling operations, and slow reaction rate etc. to achieve the effects of fast reaction and mass transfer rate, easy serialization and automation, and simple method
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Embodiment 1
[0032] 1) Weigh 1g of SiO with a diameter of 60-80nm 2 The particles were dispersed in 8 ml of toluene, and 0.1 g of propyltrimethoxysilane was added. Under the protection of nitrogen, it was stirred and refluxed at 110°C for 4 hours. After cooling, after high-speed centrifugation, toluene washing, and vacuum drying, the interface active nano-SiO can be obtained. 2 .
[0033] 2) 0.15g interface active nano-SiO 2 Disperse in 60ml toluene by ultrasonic wave, add 3ml 0.01mol / L phosphotungstic acid solution, stir to form Pickering emulsion. After milking, 0.6g of HSi(OCH 3 ) 3 Add it into the emulsion system, mix evenly, hydrolyze at 30°C for 24 hours, then let it stand, remove the upper oil phase, wash it with toluene three times, and you can get the microcapsules encapsulating the phosphotungstic acid catalyst.
[0034] 3) Slowly transfer the microcapsules of the encapsulated phosphotungstic acid catalyst prepared above to an inner diameter of 0.8cm continuous flow reactio...
Embodiment 2
[0036] 1) Weigh 1g of SiO with a diameter of 60-80nm 2 The particles were dispersed in 8 ml of toluene, and 0.6 g of propyltrimethoxysilane was added. Under the protection of nitrogen, it was stirred and refluxed at 110°C for 4 hours. After cooling, after high-speed centrifugation, toluene washing, and vacuum drying, the interface active nano-SiO can be obtained. 2 .
[0037] 2) 0.3g interface active nano-SiO 2 Disperse in 110ml of n-octane by ultrasonic wave, add 7.5ml of phosphotungstic acid solution with a concentration of 0.05mol / L, and stir to form a Pickering emulsion. After milking, 1.5g of Si(OC 2 h 5 ) 4 Add it into the emulsion system, mix well, hydrolyze at 50°C for 24 hours, then let it stand still, remove the upper oil phase, wash it with n-octane three times, and you can get the microcapsules encapsulating the phosphotungstic acid catalyst.
[0038] 3) Slowly transfer the microcapsules of the encapsulated phosphotungstic acid catalyst prepared above to a c...
Embodiment 3
[0040] 1) Weigh 1g of SiO with a diameter of 60-80nm 2 The particles were dispersed in 8 ml of toluene, and 0.3 g of propyltrimethoxysilane was added. Under nitrogen protection, stir and reflux at 110°C for 5 hours. After cooling, after high-speed centrifugation, toluene washing, and vacuum drying, the interface active nano-SiO can be obtained. 2 .
[0041] 2) 0.5g interface active nano-SiO 2 Disperse in 150ml of n-hexane by ultrasonic waves, then add 15ml of phosphotungstic acid solution with a concentration of 0.08mol / L, and stir to form a Pickering emulsion. After milking, 1.25g of Si(OCH 3 ) 4 Add it into the emulsion system, mix evenly, hydrolyze at 30°C for 24 hours, let it stand still, remove the upper oil phase, wash it with n-hexane three times, and you can get the microcapsules encapsulating the phosphotungstic acid catalyst.
[0042] 3) Slowly transfer the microcapsules of the encapsulated phosphotungstic acid catalyst prepared above to an inner diameter of 2c...
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