Method used for combined production of dimethyl-benzyl carbinol and 1,2-pentanediol
A technology of dimethyl benzyl alcohol and pentanediol, which is applied in chemical instruments and methods, preparation of hydroxyl compounds, preparation of organic compounds, etc., can solve problems affecting product concentration, difficulty in treating waste water, poor atomic economic benefits, etc., and achieves The effect of simple process and low synthesis cost
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Embodiment 1
[0047] At 90°C, a cumene solution of 1-pentene and 60% cumene hydroperoxide (the molar ratio of 1-pentene to cumene hydroperoxide is 2:1) in 2-ethylhexanoic acid The epoxidation reaction is carried out under the action of the molybdenum salt to obtain a reaction liquid containing 1,2-epoxypentane and dimethyl benzyl alcohol. The reaction solution was rectified to obtain 1,2-epoxypentane and dimethyl benzyl alcohol respectively.
[0048] At -10°C, 1,2-pentanediol with a molar ratio of 1:10 is hydrolyzed with water under the action of boron trifluoride, and rectified to obtain 1,2-pentanediol.
[0049] After calculation, the conversion rate of cumene hydroperoxide is 99.0%, the selectivity of 1,2-pentanediol is 86.3%, and the selectivity of dimethyl benzyl alcohol is 90.6%.
Embodiment 2
[0051] At 110°C, a cumene solution of 1-pentene and 60% cumene hydroperoxide (the molar ratio of 1-pentene to cumene hydroperoxide is 6:1) in 2-ethylhexanoic acid The epoxidation reaction is carried out under the action of the tungsten salt to obtain a reaction liquid containing 1,2-epoxypentane and dimethyl benzyl alcohol. The reaction solution was rectified to obtain 1,2-epoxypentane and dimethyl benzyl alcohol respectively.
[0052] At 30°C, 1,2-pentanediol with a molar ratio of 1:5 was hydrolyzed with water under the action of boron trifluoride, and rectified to obtain 1,2-pentanediol.
[0053] After calculation, the conversion rate of cumene hydroperoxide is 99.5%, the selectivity of 1,2-pentanediol is 83.3%, and the selectivity of dimethyl benzyl alcohol is 94.3%.
Embodiment 3
[0055]At 130 ° C, the cumene solution of 1-pentene and 50% cumene hydroperoxide (the molar ratio of 1-pentene to cumene hydroperoxide is 10:1) in the action of molybdenum acetylacetonate The epoxidation reaction was carried out under the following conditions to obtain a reaction liquid containing 1,2-epoxypentane and dimethyl benzyl alcohol. The reaction solution was rectified to obtain 1,2-epoxypentane and dimethyl benzyl alcohol respectively.
[0056] At 100°C, 1,2-pentanediol with a molar ratio of 1:20 is hydrolyzed with water under the action of fluoboric acid, and rectified to obtain 1,2-pentanediol.
[0057] After calculation, the conversion rate of cumene hydroperoxide is 99.9%, the selectivity of 1,2-pentanediol is 89.5%, and the selectivity of dimethyl benzyl alcohol is 97.8%.
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