Reacción #446437

ord-cf1e5c14f15142508541f085b773aefa

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe suspension is heated to +87° C.
  2. 2
    TemperaturaAfter the reaction mixture has been cooled to +15° C.
  3. 3
    Extracciónthe whole is extracted with 500 ml of methylene chloride
  4. 4
    OtroThe organic phase is separated off
  5. 5
    Secadodried over sodium sulfate
  6. 6
    workup.ADDITIONtreated with activated carbon
  7. 7
    Concentraciónconcentrated by evaporation
  8. 8
    OtroCrystallisation of the residue from ether

Procedimiento

142 g of 1-(2,2-dimethyltetralin-1-yl)-5-imidazolecarboxylic acid methyl ester are suspended in 1 liter of distilled water. The suspension is heated to +87° C. and, while stirring, a total of 335 g of ammonium peroxodisulfate is added in portions thereto within a period of 1.5 hours in such a manner that the temperature does not exceed +90° C. After the reaction mixture has been cooled to +15° C., the pH value is adjusted to pH 4 by the addition of approximately 335 g of 30% sodium hydroxide solution and the whole is extracted with 500 ml of methylene chloride. The organic phase is separated off, dried over sodium sulfate, treated with activated carbon and concentrated by evaporation. Crystallisation of the residue from ether yields 42 g of 1-(2,2-dimethyl-4-oxotetralin-1-yl)-5-imidazolecarboxylic acid methyl ester having a melting point of 93°-95° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05000777uspto-grants-1991_03