تفاعل #2348129

ord-109404c252df4d07889f21c5b087c808

معادلة التفاعل

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
المردود 29.2%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07846915B2uspto-grants-2010_12