Reaction #725899

ord-784271a49b2f4edb845d3d3c461068ce

Reaction equation

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
Yield 48.9%
O=C(COCc1ccccc1)Nc1ccc(O)cc1
2-Benzyloxy-N-(4-hydroxy-phenyl)-acetamide
Yield 48.9%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  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
    Washwashed with 5% sodium bicarbonate solution (2×100 ml), water (2×100 ml)
  5. 5
    Dryingdried over sodium sulphate
  6. 6
    workup.DISTILLATIONdistilled
  7. 7
    OtherThe crude 26 was purified by column chromatography on silica gel

Procedure

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.v1Patent: US07691364B2uspto-grants-2010_04