1-(2,3,5,6-tetrafluorophenyl)-2,2-dimethylacetone compound and its preparation method
A technology of dimethylacetone and tetrafluorophenyl, which is applied in the field of 1--2,2-dimethylacetonate and its preparation, can solve the problems of high production cost and long synthesis time, and achieve short synthesis time and low cost. Low, the effect of improving the service life
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example 1
[0026] In a 250ml four-necked round-bottomed flask equipped with a stirrer, a thermometer and a dropping funnel, add 15g of 1,2,4,5-tetrafluorobenzene (0.1mol) and 80ml of tetrahydrofuran, and freeze the mixture with liquid nitrogen acetone It is frozen to -70~-80°C.
[0027] Under vigorous stirring at -70~-80°C, 42ml of n-butyllithium hexane solution (0.105mol) was added dropwise, and the stirring was continued for 30min.
[0028] Under strong stirring at -70~-80°C, add dropwise a solution of 13.6 g of tert-butylformonitrile and 20 ml of tetrahydrofuran, continue stirring for 30 min, and slowly rise to room temperature.
[0029] Transfer the reaction solution to another 500ml round bottom flask at room temperature, add 75ml (1.1mol) of 5% dilute hydrochloric acid with stirring, heat to reflux for 30min, and cool to room temperature.
[0030] Stand at room temperature for stratification, add 20 g of anhydrous magnesium sulfate to the organic phase and stir for 1 h, filter to ...
example 2
[0034] In a 250ml four-neck round bottom flask equipped with a stirrer, a thermometer and a dropping funnel, add 16.5g of 2,3,5,6-tetrafluorobenzonitrile (0.1mol), 60ml of tetrahydrofuran, and freeze with liquid nitrogen acetone Freeze it to -70~-80°C.
[0035] Under vigorous stirring at -70~-80°C, 40ml of 16% tert-butyllithium-n-pentane solution (0.102mol) was added dropwise, continued stirring for 30min, and slowly rose to room temperature.
[0036] 75ml (1.1mol) of 5% dilute hydrochloric acid was added dropwise under stirring, heated to reflux for 30min and then cooled to room temperature.
[0037] Stand at room temperature for stratification, add 20g of anhydrous magnesium sulfate to the organic phase and stir for 1 hour, filter to remove inorganic salts, distill off the solvent from the filtrate, stop heating when crystalline solids appear, add 40ml of heptane to cool and crystallize, filter, and dry to obtain white solid crystals 19.2 g. The area percentage of GC is 99...
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