Reaktion #2829

ord-d4473f302a7441cbb178c086184f7270

Reaktionsgleichung

CCCCCCc1ccc(C(=O)N2CCOCC2)cc1[N+](=O)[O-]
compound ( [5]-(54)-75 )
CCCCCCc1ccc(C(=O)N2CCOCC2)cc1[N+](=O)[O-]
4-hexyl-3-nitrobenzoic acid morpholide
NN.O
hydrazine monohydrate
CCCCCCc1ccc(C(=O)N2CCOCC2)cc1N
compound ( [5]-(55)-75 )
Ausbeute 99.4%
CCCCCCc1ccc(C(=O)N2CCOCC2)cc1N
3-amino-4-hexylbenzoic acid morpholide
Ausbeute 99.4%

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    Filtrationthe solution was filtered through celite 545
  3. 3
    Sonstigeto remove the catalyst
  4. 4
    SonstigeThe solvent was evaporated under reduced pressure
  5. 5
    SonstigeThe residue was purified by silica gel column chromatography (Kieselgel 60=20 g, ethyl acetate)

Vorschrift

The compound ([5]-(54)-75) (700 mg) prepared in Example 62 was dissolved in ethanol (35 ml). After the solution was heated to 50° C., a suspension of 10% Pd/C (70 mg) in ethanol was added, and hydrazine monohydrate (0.35 ml) was added to the solution. The solution was stirred at 50° C. for 30 minutes. After the reaction was completed, the solution was filtered through celite 545 to remove the catalyst. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (Kieselgel 60=20 g, ethyl acetate) to obtain the above-captioned compound ([5]-(55)-75) (631 mg) as colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731310uspto-grants-1998_03