Réaction #2045006

ord-3e1294db43c247a69c9cd761403e117c

Équation de réaction

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

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurerefluxed for 80 hours
  2. 2
    workup.DISTILLATIONAcetone was distilled off
  3. 3
    workup.ADDITIONwater (3 liter) was added
  4. 4
    ExtractionCrude 16 was extracted into chloroform
  5. 5
    Séchagedried over Na2SO4
  6. 6
    workup.DISTILLATIONdistilled in hexane (750 ml)
  7. 7
    Filtrationfiltered
  8. 8
    Autrerecrystallised in methanol

Mode opératoire

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.

Source

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