Reaktion #334083

ord-5842cbd05ef742fb9086b8b1fa9a345c

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

Temperatur
130°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas placed in a 5-liter glass flask
  2. 2
    workup.STIRRINGsubsequently the resulting mixture was stirred for 1 hour
  3. 3
    Sonstigethe reaction
  4. 4
    workup.STIRRINGStirring
  5. 5
    Temperaturcool
  6. 6
    SonstigeThen an oil layer was separated
  7. 7
    workup.ADDITION200 g of ethanol was added
  8. 8
    WaschenThe resulting mixture was washed three times with each of 2 liters (l) of a 5N aqueous solution of hydrochloric acid and 2 l of saturated aqueous solution of sodium chloride
  9. 9
    Trocknendried over anhydrous sodium sulfate
  10. 10
    workup.DISTILLATIONThe unreacted phenylcyclohexane was distilled away by the use of a rotary evaporater
  11. 11
    workup.DISTILLATIONthe residue was distilled under reduced pressure
  12. 12
    Sonstigeto yield 850 g of a fraction

Vorschrift

A mixture of 3,100 grams (g) of anhydrous phenylcyclohexane, 40 g of metallic sodium and 11 g of isopropyl alcohol was placed in a 5-liter glass flask and heated to 130° C., and 650 g of styrene was dropped over 3 hours while vigorously stirring and subsequently the resulting mixture was stirred for 1 hour to complete the reaction. Stirring was stopped and the reaction mixture was allowed to stand and cool. Then an oil layer was separated and 200 g of ethanol was added. The resulting mixture was washed three times with each of 2 liters (l) of a 5N aqueous solution of hydrochloric acid and 2 l of saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The unreacted phenylcyclohexane was distilled away by the use of a rotary evaporater, and the residue was distilled under reduced pressure to yield 850 g of a fraction having a boiling point of 160°-170° C. at 0.3 mmHg (this fraction is hereinafter referred to as "Fraction f-1") and 550 g of a fraction having a boiling point of 210°-220° C. at 0.3 mmHg (this fraction is hereinafter referred to as "Fraction f-2"). An analysis confirmed that the Fraction f-1 was a compound resulting from addition of one styrene molecule to phenylcyclohexane, i.e., 1-phenyl-1-(2-phenylethyl)cyclohexane, and the Fraction f-2 was a compound resulting from addition of two styrene molecules to phenylcyclohexane, i.e., 1-phenyl-1-(2,4-diphenylbutyl)cyclohexane.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04704490uspto-grants-1987_11