Reacción #725889

ord-23114a76f8bc498c981544969feddb83

Ecuación de reacción

Cl.Nc1ccc(OCC(=O)O)cc1
(4-Aminophenoxy)acetic acid HCl
Cl.Nc1ccc(OCC(=O)O)cc1
(4-Amino-phenoxy) acetic acid HCl
Cl
HCl
CO
methanol
COC(=O)COc1ccc(N)cc1
15
Rendimiento 58.5%
COC(=O)COc1ccc(N)cc1
(4-Amino-phenoxy)-acetic acid methyl ester
Rendimiento 58.5%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat 10° C.
  2. 2
    Otrofor 1 hour
  3. 3
    Temperaturarefluxed for 10 hours
  4. 4
    workup.DISTILLATIONMethanol (3.5 liters) was distilled off
  5. 5
    workup.ADDITIONice water (1 liter) was added
  6. 6
    FiltraciónCrude 15 was filtered
  7. 7
    Otrodried
  8. 8
    Otrorecrystallised from a mixture of chloroform:hexane (1:5)

Procedimiento

To a mixture of (4-Aminophenoxy)acetic acid HCl 14 (250 g, 1.228 mol), in methanol (5 L) was passed dry HCl gas at 10° C. for 1 hour and refluxed for 10 hours. Methanol (3.5 liters) was distilled off, ice water (1 liter) was added and the pH was adjusted to 7.5 with K2CO3. Crude 15 was filtered, dried and recrystallised from a mixture of chloroform:hexane (1:5) to give pure 15 (130 g, 58.5%) as a light brown powder. The melting point was found to be 65-66.8° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07691364B2uspto-grants-2010_04