Reaktion #725889

ord-23114a76f8bc498c981544969feddb83

Reaktionsgleichung

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
Ausbeute 58.5%
COC(=O)COc1ccc(N)cc1
(4-Amino-phenoxy)-acetic acid methyl ester
Ausbeute 58.5%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat 10° C.
  2. 2
    Sonstigefor 1 hour
  3. 3
    Temperaturrefluxed for 10 hours
  4. 4
    workup.DISTILLATIONMethanol (3.5 liters) was distilled off
  5. 5
    workup.ADDITIONice water (1 liter) was added
  6. 6
    FiltrationCrude 15 was filtered
  7. 7
    Sonstigedried
  8. 8
    Sonstigerecrystallised from a mixture of chloroform:hexane (1:5)

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07691364B2uspto-grants-2010_04