Preparation method of bisphenol Z and bisphenol Z
A technology of phenol and cyclohexanone, which is applied in the field of bisphenol Z and the preparation of raw material bisphenol Z, can solve the problems of cumbersome process, adding a lot of water for cleaning, and increasing product cost, so as to achieve simple operation process, reduce the existence of salt, The effect of reducing investment costs
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Embodiment 1
[0045] Add 84.7g (0.9mol) of phenol, 29.5g (0.3mol) of cyclohexanone, 3g of catalyst Amberlyst 15 ion exchange resin, and toluene into a glass reaction flask equipped with a thermometer, a stirring device, a water separator, and a condensation reflux device. 100ml, heated to reflux (110°C), and continued heating for 6 hours. After the reaction was completed, it was cooled to room temperature and filtered. The filtered filtrate was distilled under reduced pressure to remove toluene and phenol. The crude product was recrystallized in ethanol to obtain 74.2 g of the final product with a yield of 88%. The melting point of the product was 190°C to 192°C.
Embodiment 2
[0047] 56.5g (0.6mol) of phenol, 29.5g (0.3mol) of cyclohexanone, 3g of catalyst Amberlyst 15 ion exchange resin, and 100ml of toluene were respectively added to a glass reaction bottle equipped with a thermometer and a stirring device, and the mixture was continuously stirred at room temperature for 8 hours. After the reaction was completed, the filtered filtrate was distilled under reduced pressure to remove toluene and phenol, and the crude product was recrystallized in ethanol to obtain 70.9 g of the final product with a yield of 92% and a melting point of 190°C to 192°C.
Embodiment 3
[0049]Add 56.5g (0.6mol) of phenol, 29.5g (0.3mol) of cyclohexanone, 3g of catalyst Amberlyst 15 ion exchange resin, and xylene respectively 100ml, heated to 80°C for 4 hours. After the reaction was completed, it was lowered to room temperature, filtered, and the filtered filtrate was distilled under reduced pressure to remove xylene and phenol, and the crude product was recrystallized in ethyl acetate to obtain 64.4 g of the final product with a yield of 80%. The melting point of the product was 190° C. to 192 ℃.
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