Reaktion #934611

ord-037422849bb14eb0bffbce1c75143033

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe mixture was reacted at 140° C. under a reduced pressure of 20 mmHg for 4 hours
  2. 2
    TemperaturAfter cooling
  3. 3
    Sonstigethe reaction product was crystallized from n-hexane

Vorschrift

The phenyl ester (14.8 g) synthesized in (2) above was mixed with 3-(2,4-di-t-pentylphenoxy)propylamine (14.6 g), and the mixture was reacted at 140° C. under a reduced pressure of 20 mmHg for 4 hours. After cooling, the reaction product was crystallized from n-hexane to obtain 3,6-dihydroxy-4-[3-(2,4-di-t-pentylphenoxy)propylcarbamoyl]benzonorbornene. (Yield: 15.1 g (61.2 %), m.p.: 142° C.)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05142029uspto-grants-1992_08