Reaktion #1831454

ord-5d615dc0d391490cb063e8c10c01152d

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was heated
  2. 2
    Temperaturunder reflux for 6 hours
  3. 3
    EinengenThe reaction mixture was concentrated under reduced pressure
  4. 4
    SonstigeThe resulting residue was purified by silica gel column chromatography (a eluting solvent

Vorschrift

3-[(4,4,4-Trifluoro-3-oxo-1-butenyl)amino]-2propenenitrile (a mixture of IIa and IIb; 1.90 g, 10 mmol) was dissolved in methanol (15 ml), and sodium hydroxide (600 mg, 15 mmol) was added. The mixture was heated under reflux for 6 hours. The reaction mixture was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (a eluting solvent: hexane/acetone=1/1) to obtain 1.25 g (yield 65.6%) of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07015236B2uspto-grants-2006_03