Reacción #40269

ord-4ee3e8ab5fd74d1e987263adc9c61aec

Ecuación de reacción

Nc1ccc(CCCC(=O)O)cc1
4-(4-Aminophenyl)butyric acid
CO
methanol
Cl
hydrogen chloride
COC(=O)CCCc1ccc(N)cc1.Cl
methyl 4-(4-aminophenyl)butyrate hydrogen chloride

Condiciones de reacción

Temperatura
85°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas bubbled through the solution
  2. 2
    TemperaturaAfter the reaction mixture was cooled to room temperature
  3. 3
    workup.ADDITIONethyl ether (100 ml.) was added
  4. 4
    OtroThe mixture, which separated into two layers
  5. 5
    FiltraciónThe crystalline product was collected by filtration
  6. 6
    Otrodried thoroughly
  7. 7
    OtroThe filtrate was evaporated to dryness
  8. 8
    Otrothe residue was recrystallized from MeOH/benzene

Procedimiento

4-(4-Aminophenyl)butyric acid (5 g) was dissolved in 40 ml methanol. The solution was refluxed at 80-90° C. with stirring for 4 h while hydrogen chloride gas was bubbled through the solution. After the reaction mixture was cooled to room temperature, ethyl ether (100 ml.) was added. The mixture, which separated into two layers, was refrigerated overnight. The crystalline product was collected by filtration and dried thoroughly. The filtrate was evaporated to dryness and the residue was recrystallized from MeOH/benzene. The total amount of the product methyl 4-(4-aminophenyl)butyrate hydrogen chloride obtained was 5.6 g (87.5%), m.p. 143-145° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07727558B2uspto-grants-2010_06