Reaktion #96152

ord-b7d7c3da97f04a1abc3a4b39914cecbd

Reaktionsgleichung

Oc1ccccc1
phenol
C=C(C)c1ccccc1
α-methylstyrene
CC(C)(c1ccccc1)c1ccc(O)c(C(C)(C)c2ccccc2)c1
2,4-Di-(α,α-dimethylbenzyl)phenol

Lösungsmittel

Reaktionsbedingungen

Temperatur
140°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was cooled to 110° C.
  2. 2
    WaschenAfter washing the resulting solution at 80° C. with 750 ml of an aqueous solution of 37.5 grams of sodium carbonate and 75 grams of sodium chloride
  3. 3
    Waschenthe organic phase was washed thrice with 1000 ml of aqueous sodium chloride solution
  4. 4
    Trocknenthen dried over anhydrous sodium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    workup.DISTILLATIONvacuum distilled
  7. 7
    SonstigeThe above-named product was obtained as the main fraction boiling at 172°-175° C./0.15-0.18 mm Hg in a yield of 1229.8 grams (49.6% of theory)

Vorschrift

This intermediate was made by the general procedure of U.S. Pat. No. 2,714,120 by reacting a mixture of 705.8 grams (7.5 moles) of phenol with 1772.7 grams (15 moles) of α-methylstyrene in the presence of 25.7 grams (0.135 moles) of p-toluenesulfonic acid monohydrate catalyst. This mixture was heated under nitrogen at 140° C. for 2.5 hours. The reaction mixture was cooled to 110° C. and 1125 ml of toluene was added. After washing the resulting solution at 80° C. with 750 ml of an aqueous solution of 37.5 grams of sodium carbonate and 75 grams of sodium chloride, the organic phase was washed thrice with 1000 ml of aqueous sodium chloride solution; then dried over anhydrous sodium sulfate; filtered and vacuum distilled. The above-named product was obtained as the main fraction boiling at 172°-175° C./0.15-0.18 mm Hg in a yield of 1229.8 grams (49.6% of theory). The product melted at 63°-65° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04347180uspto-grants-1982_08