Reacción #725890

ord-b329edd0254a4c839d8fceb76e577bbb

Ecuación de reacción

COC(=O)C(C)Cl
methyl 2-chloropropionate
CC(=O)Nc1ccc(O)cc1
Paracetamol
O=C([O-])[O-].[K+].[K+]
K2CO3
[I-].[Na+]
sodium iodide
COC(=O)C(C)Oc1ccc(NC(C)=O)cc1
16
COC(=O)C(C)Oc1ccc(NC(C)=O)cc1
2-(4-Acetylamino-phenoxy)-propionic acid methyl ester

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturarefluxed for 80 hours
  2. 2
    workup.DISTILLATIONAcetone was distilled off
  3. 3
    workup.ADDITIONwater (3 liter) was added
  4. 4
    ExtracciónCrude 16 was extracted into chloroform
  5. 5
    Secadodried over Na2SO4
  6. 6
    workup.DISTILLATIONdistilled in hexane (750 ml)
  7. 7
    Filtraciónfiltered
  8. 8
    Otrorecrystallised in methanol

Procedimiento

To a mixture of Paracetamol (150 grams, 992 mmol), anhydrous K2CO3 (540 Kg, 3.91 mol) and sodium iodide (18 g, 120 mmol) in anhydrous acetone (3 liters) was added methyl 2-chloropropionate (180 g, 1.469 mmol) and refluxed for 80 hours. Acetone was distilled off and water (3 liter) was added. Crude 16 was extracted into chloroform, dried over Na2SO4, distilled in hexane (750 ml), filtered and recrystallised in methanol to give pure 16 (95 g, 40.4%) as a white powder. The melting point was found to be 96.5-98.2° C. The product was tested by HPLC and found to be 99%+pure. The structure was confirmed with NMR.

Fuente

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