Реакция #10042

Уравнение реакции

cyclohexene

cyclohexene

cyclohexanol

Cyclohexene

→

methylcyclopentene

cyclohexanol

Растворители

water

Условия реакции

Обработка

1. 1
   ДругоеWith respect to the manner of the hydration reaction, there
2. 2
   Другоеthe reaction
3. 3
   ДругоеThe hydration reaction
4. 4
   Другоеto obtain a reaction mixture
5. 5
   Другоеproduced
6. 6
   ДругоеThe oil phase is phase-separated from the aqueous phase
7. 7
   Другоеprovided to a separation step
8. 8
   workup.ADDITIONThe aqueous phase containing the hydration catalyst
9. 9
   ДругоеIn the hydration reaction

Методика

With respect to the manner of the hydration reaction, there is no particular limitation; the reaction can be performed in either of continuous and batchwise manners. The hydration reaction is generally performed as follows. Cyclohexene is added to a catalyst slurry comprising a hydration catalyst and water to effect hydration of cyclohexene in a suspension state to obtain a reaction mixture comprising an aqueous phase comprised of the catalyst slurry and an oil phase comprised of cyclohexanol produced and the cyclohexene remaining unreacted. The oil phase is phase-separated from the aqueous phase, and provided to a separation step. The aqueous phase containing the hydration catalyst can be recycled as the catalyst slurry to the reactor. In the hydration reaction, a small amount of methylcyclopentene is generally formed as a by-product as well as cyclohexanol as the desired intermediate. The oil phase, which contains the cyclohexanol, the methylcyclopentene and the cyclohexene, is separated into a high boiling point component containing cyclohexanol and a low boiling point component containing cyclohexene by a customary method, such as distillation. If desired, the separated cyclohexanol can be further subjected to treatment for isolation, thereby obtaining a cyclohexanol having a desired purity. In such a case, it is preferred that the obtained cyclohexanol has a purity of 99% or more. In general, it is preferred that the unreacted cyclohexene which is separated from cyclohexanol is subjected to treatment for isolation so as to obtain cyclohexene having a desired purity, followed by recycling thereof to the reactor.

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