Réaction #2006410

ord-16f2c8cfa26d4881a2ce547cd7871669

Équation de réaction

Nc1ccc(CC(=O)O)cc1
4-aminophenylacetic acid
Cl
HCl
CO
methanol
COC(=O)Cc1ccc(N)cc1
3
Rendement 74.0%
COC(=O)Cc1ccc(N)cc1
Methyl-4-aminophenylacetate
Rendement 74.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction mixture was then quenched with a saturated aqueous solution of NaHCO3
  2. 2
    AutreThe methanol was evaporated under reduced pressure
  3. 3
    Extractionthe aqueous layer was extracted several times with AcOEt
  4. 4
    SéchageThe combined organic extracts were dried over (MgSO4)
  5. 5
    Autreevaporated
  6. 6
    AutreThe crude residue was purified by flash chromatography

Mode opératoire

To a solution of 4-aminophenylacetic acid (10 g, 66.2 mmol) in methanol (150 mL) at room temperature was added HCl conc. (37% 25 mL). The mixture became yellow and was stirred overnight. The reaction mixture was then quenched with a saturated aqueous solution of NaHCO3. The methanol was evaporated under reduced pressure and the aqueous layer was extracted several times with AcOEt. The combined organic extracts were dried over (MgSO4) and evaporated. The crude residue was purified by flash chromatography using hexane/AcOEt (4:1) as solvent mixture yielding 3 as a yellow oil (9.44 g, 74%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE043343E1uspto-grants-2012_05