Reacción #2348130

ord-e413f568739645b2a2c5c47fc11a3307

Ecuación de reacción

O=C(O)c1ccc(O)cc1
4-Hydroxybenzoic acid
Nc1ccc(O)cc1
4-aminophenol
CCN=C=NCCCN(C)C
EDCI
O=C(Nc1ccc(O)cc1)c1ccc(O)cc1
4-hydroxy-N-(4-hydroxyphenyl)-benzamide
Rendimiento 34.6%

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07846915B2uspto-grants-2010_12