Reaction #2348130

ord-e413f568739645b2a2c5c47fc11a3307

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe reaction mixture was then partitioned between EtOAc (200 mL) and water (200 mL)
  2. 2
    OtherThe organic layer was separated
  3. 3
    Washwashed consecutively with 1 N HCl, water, saturated sodium bicarbonate solution, water, and brine
  4. 4
    Dryingdried over MgSO4
  5. 5
    OtherSolvent was removed under reduced pressure
  6. 6
    Otherthe crude product was purified by column chromatography

Procedure

4-Hydroxybenzoic acid (1.01 g, 7.31 mmol) and 4-aminophenol (1.19 g, 10.9 mmol) were dissolved in 15 mL of dry DMF. To the above solution EDCI (1.40 g, 7.31 mmoL) was added in one portion and the resulting mixture was stirred at rt overnight under nitrogen. The reaction mixture was then partitioned between EtOAc (200 mL) and water (200 mL). The organic layer was separated, washed consecutively with 1 N HCl, water, saturated sodium bicarbonate solution, water, and brine, and dried over MgSO4. Solvent was removed under reduced pressure and the crude product was purified by column chromatography using EtOAc in hexane as an eluent (10% to 20%) to give 580 mg (34% yield) of 4-hydroxy-N-(4-hydroxyphenyl)-benzamide. MS (ES) m/z: 230.04 (M+1).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07846915B2uspto-grants-2010_12