Réaction #2045005

ord-7432d99ecb824b71b9131da5cf7d3322

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreat 10° C.
  2. 2
    Autrefor 1 hour
  3. 3
    Températurerefluxed 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
    Autredried
  8. 8
    Autrerecrystallised from a mixture of chloroform:hexane (1:5)

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08409559B2uspto-grants-2013_04