Reaktion #573594

ord-c9fc8a668fe5448c9f1ababde1774eaf

Reaktionsbedingungen

Temperatur
35°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    Temperaturthe temperature maintained for an additional 2.5 hours
  3. 3
    TemperaturThe solution was then cooled to 5° C.
  4. 4
    Sonstigequenched with water
  5. 5
    WaschenAfter transfer to a separatory funnel, the solution was washed with water
  6. 6
    Trocknentwice with brine, dried over anhydrous sodium sulfate
  7. 7
    Sonstigerotary evaporated

Vorschrift

The starting material 1,1,4,4,7-pentamethyl-5-methoxy-1,2,3,4-tetrahydronaphthalene was prepared as follows. First, a 500 flask was charged with 230 ml dichloromethane, 19 g TiCl4, and 18.3 g 2,5-dichloro-2,5-dimethylhexane, at 22° C. Next, 3-methyl anisole (12.2 g in 20 ml dichloromethane) was added dropwise over a period of an hour. After the addition was completed, the solution was heated to 35° C. and the temperature maintained for an additional 2.5 hours. The solution was then cooled to 5° C. and quenched with water. After transfer to a separatory funnel, the solution was washed with water, then twice with brine, dried over anhydrous sodium sulfate, and rotary evaporated to give a crude product (23.78 g) containing 79.4% (by area % GC) of 1,1,4,4,7-pentamethyl-5-methoxy-1,2,3,4-tetrahydronaphthalene.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05292719uspto-grants-1994_03