Reaktion #1273169

ord-15212c28defa4df88e6588c79f58b0b5

Lösungsmittel

Reaktionsbedingungen

Temperatur
3°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter the dropwise addition
  2. 2
    workup.STIRRINGthe mixture was stirred for 5 hours at room temperature
  3. 3
    ExtraktionAn organic phase was extracted
  4. 4
    workup.DISTILLATIONthe obtained organic phase was distilled off at reduced pressure at 40° C
  5. 5
    workup.DISTILLATIONAfter further distilling off at reduced pressure at 170° C.
  6. 6
    Temperaturthe organic phase was cooled to room temperature
  7. 7
    workup.ADDITION50 ml of acetone was introduced
  8. 8
    Sonstigerecrystallized
  9. 9
    FiltrationThe precipitated crystals were filtered off

Vorschrift

To 20.0 g of benzene, 6.83 g of aluminum chloride was added, cooled by 3° C. and stirred, and 40.4 g of cyclohexyl chloride was slowly added dropwise. After the dropwise addition, the mixture was stirred for 5 hours at room temperature and was poured into ice water. An organic phase was extracted using ethyl acetate and the obtained organic phase was distilled off at reduced pressure at 40° C. After further distilling off at reduced pressure at 170° C., the organic phase was cooled to room temperature, 50 ml of acetone was introduced and recrystallized. The precipitated crystals were filtered off and 14 g of tricyclohexylbenzene was obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08673538B2uspto-grants-2014_03