反应 #2348129

ord-109404c252df4d07889f21c5b087c808

反应方程式

O=C(O)c1ccc(O)cc1
4-Hydroxybenzoic acid
Nc1ccccc1
aniline
CCN=C=NCCCN(C)C
EDCI
O=C(Nc1ccccc1)c1ccc(O)cc1
4-Hydroxy-N-phenyl-benzamide
收率 29.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The reaction mixture was then partitioned between EtOAc (200 mL) and water (200 mL)
  2. 2
    其他The organic layer was separated
  3. 3
    洗涤washed consecutively with 1 N HCl, water, saturated sodium bicarbonate solution, water, and brine
  4. 4
    干燥dried over MgSO4
  5. 5
    其他Solvent was removed under reduced pressure
  6. 6
    其他the crude product was purified by column chromatography

实验过程

4-Hydroxybenzoic acid (1.1 g, 7.96 mmoL) and aniline (742 mg, 7.23 mmol) were dissolved in 20 mL of dry DMF. To the above solution EDCI (1.53 g, 7.23 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 10% EtOAc in hexane to give 450 mg (29% yield) of 4-Hydroxy-N-phenyl-benzamide. MS (ES) m/z: 214.08 (M+1).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07846915B2uspto-grants-2010_12