反応 #10042

ord-5a2db9b125ed4b8db32b988a6303e957

反応方程式

C1=CCCCC1
cyclohexene
C1=CCCCC1
cyclohexene
OC1CCCCC1
cyclohexanol
C1=CCCCC1
Cyclohexene
CC1=CCCC1
methylcyclopentene
OC1CCCCC1
cyclohexanol

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他With respect to the manner of the hydration reaction, there
  2. 2
    その他the reaction
  3. 3
    その他The hydration reaction
  4. 4
    その他to obtain a reaction mixture
  5. 5
    その他produced
  6. 6
    その他The oil phase is phase-separated from the aqueous phase
  7. 7
    その他provided to a separation step
  8. 8
    workup.ADDITIONThe aqueous phase containing the hydration catalyst
  9. 9
    その他In the hydration reaction

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07091381B2uspto-grants-2006_08