Réaction #2045015

ord-b1893d7b580a49718678470051e47742

Équation de réaction

Nc1ccc(O)cc1
4-aminophenol
O=C([O-])O.[Na+]
sodium bicarbonate
O=C(Cl)COCc1ccccc1
benzyloxy acetyl chloride
O=C(COCc1ccccc1)Nc1ccc(O)cc1
26
Rendement 48.9%
O=C(COCc1ccccc1)Nc1ccc(O)cc1
2-Benzyloxy-N-(4-hydroxy-phenyl)-acetamide
Rendement 48.9%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe solids were filtered off
  2. 2
    workup.ADDITIONcold water (500 ml) was added
  3. 3
    ExtractionCrude 26 was extracted into chloroform
  4. 4
    Lavagewashed with 5% sodium bicarbonate solution (2×100 ml), water (2×100 ml)
  5. 5
    Séchagedried over sodium sulphate
  6. 6
    workup.DISTILLATIONdistilled
  7. 7
    AutreThe crude 26 was purified by column chromatography on silica gel

Mode opératoire

To mixture of 4-aminophenol (20 g, 183.2 mmol) and sodium bicarbonate (17 grams, 202 mmol) in acetone (150 ml) at 0° C. was added benzyloxy acetyl chloride (40 g, 216.8 mmol) drop wise, followed by stirring at room temperature for 20 hours. The solids were filtered off, and cold water (500 ml) was added. Crude 26 was extracted into chloroform, washed with 5% sodium bicarbonate solution (2×100 ml), water (2×100 ml), dried over sodium sulphate and distilled. The crude 26 was purified by column chromatography on silica gel using chloroform as eluant to get pure 26 (23 g, 48.9%) as a light orange syrup.

Source

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