Reaktion #41196

ord-8077ea87bc5b4e968bb24e3cbfde846c

Reaktionsgleichung

O=C1CCC1
cyclobutanone
CC(C)(C)OC(=O)NN
hydrazinecarboxylic acid tert-butyl ester
CC(C)(C)OC(=O)NN=C1CCC1
N′-cyclobutylidene-hydrazinecarboxylic acid tert-butyl ester
Ausbeute 81.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturto reflux for 2 hours
  3. 3
    TemperaturAfter cooling down
  4. 4
    Sonstigea precipitate formed
  5. 5
    Filtrationthe solid was filtered under vacuum
  6. 6
    workup.ADDITIONIsopropanol (10 mL) and hexane (100 mL) were added to the solid
  7. 7
    Sonstigethe mixture was put on the rotary evaporator under vacuum until a slurry
  8. 8
    FiltrationAfter filtration
  9. 9
    Waschenthe solid was washed with hexane twice
  10. 10
    Sonstigedried in vacuo

Vorschrift

The reaction mixture of cyclobutanone (15 g, 214 mmol) and hydrazinecarboxylic acid tert-butyl ester (28.3 g, 214 mmol) in hexane (225 mL) was heated to reflux for 2 hours. After cooling down, a precipitate formed and the solid was filtered under vacuum. Isopropanol (10 mL) and hexane (100 mL) were added to the solid and the mixture was put on the rotary evaporator under vacuum until a slurry was generated. After filtration, the solid was washed with hexane twice and dried in vacuo to afford N′-cyclobutylidene-hydrazinecarboxylic acid tert-butyl ester (32 g, 81%) as white solid which was used without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728029B2uspto-grants-2010_06