Reaktion #831104

ord-2304c98036244104891982e779d77ca3

Reaktionsgleichung

C=Cc1ccc(O)cc1
4-hydroxystyrene
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
C=COC(C)(C)C
tert-butyl vinyl ether
C=Cc1ccc(OC(C)OC(C)(C)C)cc1
desired product
C=Cc1ccc(OC(C)OC(C)(C)C)cc1
1-(4-vinylphenoxy)-1-tert-butoxyethane

Lösungsmittel

Reaktionsbedingungen

Temperatur
10°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture is cooled to between 0° and 5° C.
  2. 2
    WaschenThe reaction mixture is washed three times with 150 ml of 1N NaOH and three times with demineralized water

Vorschrift

12.02 g (100 mmol) of 4-hydroxystyrene, 0.09 g of p-toluenesulfonic acid and 100 ml of diethyl ether are introduced under a nitrogen atmosphere into a 250 ml three-neck flask. The mixture is cooled to between 0° and 5° C., and 11.02 g (110 mmol) of tert-butyl vinyl ether are added dropwise at this temperature over the course of 15 minutes. The mixture is then stirred at 10° C. for 2 hours. The reaction mixture is washed three times with 150 ml of 1N NaOH and three times with demineralized water. Stripping off of the solvent gives 16 g (72% of theory) of the desired product in the form of a yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05558978uspto-grants-1996_09