تفاعل #725876

ord-2943e09b6f01470994048c2a5a8ef084

معادلة التفاعل

CCO
EtOH
Cc1ccccc1S(=O)(=O)n1cccc1C(=O)c1ccc(NC(=O)C(F)(F)F)cc1
N-toluenesulfonyl-2-(4-(trifluoroacetylamino)benzoyl)pyrrole
[K+].[OH-]
KOH
Nc1ccc(C(=O)c2ccc[nH]2)cc1
2-(4-aminobenzoyl)pyrrole
المردود 94.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was heated
  2. 2
    درجة الحرارةat reflux until thin layer chromatography (TLC) analysis
  3. 3
    أخرىthe mixture was evaporated to dryness
  4. 4
    أخرىThe crude product was purified by column chromatography (SiO2, EtOAc:Hexanes)

الإجراء التجريبي

To a stirred EtOH (4 mL) solution containing N-toluenesulfonyl-2-(4-(trifluoroacetylamino)benzoyl)pyrrole (0.500 g, 1.15 mmol), was added 40% KOH solution (2 mL) and the mixture was heated at reflux until thin layer chromatography (TLC) analysis showed complete conversion of the starting material. The resulting solution was cooled to room temperature and diluted with EtOAc (20 mL), and the mixture was evaporated to dryness. The crude product was purified by column chromatography (SiO2, EtOAc:Hexanes) to afford the purified product 2-(4-aminobenzoyl)pyrrole (196 mg, 94% yield). 1H NMR (400 MHz, CD2Cl2, 25° C.) δ4.19 (bs, 2H), 6.33 (m, 1H), 6.72 (d, 2H), 6.88 (m, 1H), 7.10 (m, 1H), 7.82 (d, 2H), 9.90 (bs, 1H); 13C NMR (100 MHz, CD2Cl2, 25° C.) δ110.9, 114.2, 118.0, 124.5, 128.5, 131.8, 131.9, 151.3, 183.5; HRMS (EI): m/z 186.0793 (100) {M}+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07691292B2uspto-grants-2010_04