Reacción #5869

ord-37a0638f1dc84d4298b53e5aaef50245

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe suspension is heated to +87° C.
  2. 2
    workup.ADDITIONwithin a period of 1.5 hours a total of 335 g of ammoniaperoxodisulfate is added portionwise in such a manner
  3. 3
    Otrodoes not exceed +90° C
  4. 4
    TemperaturaAfter cooling the reaction mixture to +15° C.
  5. 5
    ExtracciónThe mixture is extracted with 500 ml of methylene chloride
  6. 6
    OtroThe organic phase is separated
  7. 7
    Secadodried with sodium sulfate
  8. 8
    workup.ADDITIONtreated with activated carbon
  9. 9
    Concentraciónconcentrated
  10. 10
    OtroCrystallisation of the residue from diethyl ether

Procedimiento

142 g of 1-(2,2-dimethyl-tetralin-1-yl)-5-imidazolecarboxylic acid methyl ester are dispersed in 1 liter of deionisized water. The suspension is heated to +87° C., and within a period of 1.5 hours a total of 335 g of ammoniaperoxodisulfate is added portionwise in such a manner, that the temperature does not exceed +90° C. After cooling the reaction mixture to +15° C., the pH-value is adjusted to pH 4 by addition of 335 g of a sodium hydroxide solution 30%. The mixture is extracted with 500 ml of methylene chloride. The organic phase is separated, dried with sodium sulfate, treated with activated carbon and concentrated. Crystallisation of the residue from diethyl ether yields 42 g of 1-(2,2-dimethyl-4-oxo-tetralin-1-yl)-5-imidazolecarboxylic acid methyl ester, having a melting point of 93°-95° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05246915uspto-grants-1993_09