Reaktion #69938

ord-69e317fd0d0c49f4b00d938a29029421

Reaktionsgleichung

COC(=O)c1ccc(O)cc1
Methyl 4-hydroxy-benzoate
CC(C)N(CCC(O)c1ccccc1)C(C)C
3-Diisopropylamino-1-phenyl-propan-1-ol
COC(=O)c1ccc(O)c(C(CCN(C(C)C)C(C)C)c2ccccc2)c1
product
Ausbeute 92.0%
COC(=O)c1ccc(O)c(C(CCN(C(C)C)C(C)C)c2ccccc2)c1
methyl 3-(3-diisopropylamino-1-phenyl-propyl)-4-hydroxy-benzoate
Ausbeute 92.0%

Reaktionsbedingungen

Temperatur
52.5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe mixture is reacted while hot for 5-6 hours
  2. 2
    TemperaturThe mixture is cooled at room temperature
  3. 3
    ExtraktionThe product is extracted with dichloromethane (200 ml)
  4. 4
    Waschenthe organic phase is washed with a 10% sodium hydroxide solution (2×100 ml)

Vorschrift

Methyl 4-hydroxy-benzoate (52.0 g, 340 mmol) is suspended in methanesulfonic acid (90 ml) in a round-bottom flask under inert atmosphere and the mixture is heated at a temperature of 50-55° C. 3-Diisopropylamino-1-phenyl-propan-1-ol (20.0 g, 85.0 mmol) is slowly added in about 2 hours and the mixture is reacted while hot for 5-6 hours. The mixture is cooled at room temperature and slowly poured in ice/water (200 g) under strong stirring. The product is extracted with dichloromethane (200 ml) and the organic phase is washed with a 10% sodium hydroxide solution (2×100 ml), then with an ammonium chloride aqueous solution until neutral pH. 28.9 g of a product are obtained in 92% yield.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530691B2uspto-grants-2013_09