Reaktion #3043

ord-5ea8ac69bd1848ae813a64e74a7a7adf

Reaktionsgleichung

CC(=O)Cl
acetylchloride
Cl
hydrochloric acid
CC(C)(C)c1cccc(C(C)(C)C)c1O
2,6-di-t-butylphenol
CC(=O)c1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1
desired subtitled intermediate
CC(=O)c1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1
1-[3,5-bis(1,1-dimethylethyl) -4-hydroxyphenyl]ethanone

Lösungsmittel

Reaktionsbedingungen

Temperatur
-4°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe mixture separated into layers which
  2. 2
    Sonstigewere subsequently separated
  3. 3
    WaschenThe organic layer was washed with 100 ml of saturated sodium bicarbonate and 100 ml of brine
  4. 4
    SonstigeThe organic layer was dried
  5. 5
    Sonstigethe solvent evaporated

Vorschrift

Under a nitrogen atmosphere, 6.89 ml of acetylchloride and 14.75 ml of stannic chloride were dissolved in 200 ml of methylene chloride and chilled to -4° C. To this was added 20 g of 2,6-di-t-butylphenol (in 100 ml of methylene chloride) over 10 minutes. The resultant mixture was stirred for 30 minutes at 0° C., then poured into a mixture of 400 ml of ice and 1N hydrochloric acid and stirred. The mixture separated into layers which were subsequently separated. The organic layer was washed with 100 ml of saturated sodium bicarbonate and 100 ml of brine. The organic layer was dried and the solvent evaporated to give 23.39 g of the desired subtitled intermediate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731336uspto-grants-1998_03