Reaktion #1702063

ord-5882c151337f4c049761ccbd9576fef9

Reaktionsgleichung

[Al+3].[Cl-].[Cl-].[Cl-]
AlCl3
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
Oc1ccccc1
phenol
ClCCl
dichloromethane
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
CC(C)(Cl)CCC(C)(C)Cl
2,5-dichloro-2,5-dimethylhexane
CC1(C)CCC(C)(C)c2cc(O)ccc21
5,6,7,8-tetrahydro-2-hydroxy-5,5,8,8-tetramethyl naphthalene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted by ethyl acetate
  2. 2
    WaschenThe organic layer was washed by water
  3. 3
    Trocknena saturated sodium hydrogen carbonate aq. solution, and a saturated saline solution, dried over magnesium sulfate
  4. 4
    Einengenconcentrated under reduced pressure
  5. 5
    SonstigeThe crude product was purified by recrystallization in a solvent of hexane

Vorschrift

The synthesis process is as set forth in the chemical reaction formula below. The AlCl3 in the reaction path stands for aluminum chloride. Into phenol (1.02 g, 10.8 mmol) were added anhydrous dichloromethane (5 mL), aluminum chloride (144 mg, 1.08 mmol), and 2,5-dichloro-2,5-dimethylhexane (2.18 g, 11.9 mmol) followed by stirring at room temperature for 19 hours. The reaction solution was poured into cold water and extracted by ethyl acetate. The organic layer was washed by water, a saturated sodium hydrogen carbonate aq. solution, and a saturated saline solution, dried over magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by recrystallization in a solvent of hexane. The yield was 1.83 g (83%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08765719B2uspto-grants-2014_07