Method for catalytically preparing propylene monothio-carbonate by ionic liquid
A technology of propylene monothiocarbonate and ionic liquid, which is applied in the field of ionic liquid catalyzed preparation of propylene monothiocarbonate, can solve the problems that ionic liquid catalysts have not yet been developed and applied, and achieve improved selectivity and conversion, reaction The effect of mild conditions and simple operation
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Embodiment 1
[0020] Add 2 grams of propylene oxide in a 10ml autoclave, add 1-butyl-3-methylimidazolium bromide borate ionic liquid catalyst by 2% of the mass of propylene oxide, under uniform stirring, feed carbon oxysulfide to 2 MPa pressure, reacted at 100°C for 1 hour, slowly degassed after cooling to room temperature, filtered to obtain the crude product liquid, and obtained propylene monothiocarbonate by distillation under reduced pressure, and the yield was measured by hydrogen nuclear magnetic spectrum, monothiocarbonic acid The yield results of propylene ester products are shown in Table 1 below.
Embodiment 2
[0022] Add 2 grams of propylene oxide in a 10ml autoclave, add 1-butyl-3-methylimidazolium fluoroborate ionic liquid catalyst according to 0.5% of the mass of propylene oxide, stir evenly, and feed carbon oxysulfide to 3 MPa pressure, react at 80°C for 2 hours, slowly release gas after cooling to room temperature, filter to obtain crude product liquid, obtain propylene monothiocarbonate through vacuum distillation, and measure the yield by hydrogen nuclear magnetic spectrum, monothiocarbonic acid The yield results of propylene ester products are shown in Table 1 below.
Embodiment 3
[0024] Add 2 grams of propylene oxide into a 10ml autoclave, add 1-butyl-3-methylimidazolium fluorophosphate ionic liquid catalyst according to 0.1% of the mass of propylene oxide, stir evenly, and feed carbon oxysulfide to 5 MPa pressure, reacted at 70°C for 6 hours, cooled to room temperature and slowly released gas, filtered to obtain the crude product liquid, and obtained monothiopropylene carbonate through vacuum distillation, and the yield was measured by nuclear magnetic hydrogen spectrum, monothiopropylene The ester product yield results are shown in Table 1 below.
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