Réaction #349524

ord-d344f51264274e48a11f7c3042dc145a

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction was heated
  2. 2
    Températureto reflux for 17 hours
  3. 3
    Températurecooled
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    workup.ADDITIONpotassium t-butoxide added
  6. 6
    Températurethe mixture heated
  7. 7
    Températureto reflux for 8 hours
  8. 8
    workup.ADDITIONThe reaction was poured over ice and brine and toluene
  9. 9
    workup.ADDITIONadded
  10. 10
    AutreThe toluene phase was separated
  11. 11
    Séchagedried over Na2SO4
  12. 12
    ExtractionThe aqueous phase was extracted well with CH2Cl2
  13. 13
    Séchagethe combined extracts dried over Na2SO4
  14. 14
    Concentrationconcentrated
  15. 15
    Autrethe crude product recrystallized from THF/hexane
  16. 16
    Autreto give the desired end product, mp 258°-261°
  17. 17
    Autrewas obtained as colorless crystals

Mode opératoire

To a solution of 3.43 g. (10.15 mmol) of the end product of Example 15 in 60 ml. of absolute EtOH, was added 12 ml. of hydrazine-hydrate. The reaction was heated to reflux for 17 hours, then cooled and concentrated in vacuo. The residue was taken up in 60 ml. toluene; 1.0 g. potassium t-butoxide added and the mixture heated to reflux for 8 hours, then cooled to room temperature and stirred for 9 hours. The reaction was poured over ice and brine and toluene added. The toluene phase was separated and dried over Na2SO4. The aqueous phase was extracted well with CH2Cl2 and the combined extracts dried over Na2SO4. The dried solutions were combined and concentrated and the crude product recrystallized from THF/hexane to give the desired end product, mp 258°-261°. An analytical sample was prepared by an additional recrystallization from THF/hexane and was obtained as colorless crystals: mp 259°-261°.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04153799uspto-grants-1979_05