Reacción #7923

ord-939af69376254c7286149b31bfef6201

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was evaporated under vacuum to an oil which
  2. 2
    Lavadowashed with 1N HCl (2×6 ml), water (6 mL) and brine (6 ml)
  3. 3
    Secadodried over MgSO4
  4. 4
    Filtraciónfiltered
  5. 5
    Otroevaporated under vacuum

Procedimiento

A solution of 9a-butyl-7-hydroxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (60 mg, 0.22 mmol) and hydroxyl amine hydrochloride (77 mg, 1.11 mmol) in anhydrous pyridine (0.5 mL) was stirred under a nitrogen atmosphere at room temperature for 4.3 hours and then heated in an oil bath at 60° C. for 30 minutes. The reaction mixture was evaporated under vacuum to an oil which was taken up in EtOAc (10 mL), washed with 1N HCl (2×6 ml), water (6 mL) and brine (6 ml), dried over MgSO4, filtered, and evaporated under vacuum. The residue was lyophilized from benzene (3 mL) to afford (3E)-9a-butyl-7-hydroxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one oxime as an amorphous solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087599B2uspto-grants-2006_08