Acetic Acid → O-Ethylacetanilide

HRID 711751

Reaktionsgleichung

Reaktionsgleichung von HRID 711751
[CH2:1]([C:3]1[CH:9]=[CH:8][CH:7]=[CH:6][C:4]=1[NH2:5])[CH3:2].[CH3:10][C:11](O)=[O:12].C(OC(=O)C)(=O)C.O>CCO>[CH2:1]([C:3]1[CH:9]=[CH:8][CH:7]=[CH:6][C:4]=1[NH:5][C:11](=[O:12])[CH3:10])[CH3:2]

Komponenten

6

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

2-Ethylaniline (9.70 g, 80.0 mmol) was added to a mixture of glacial AcOH (30 mL) and acetic anhydride (20 mL), and the resulting mixture was refluxed at 120° C. for 3 h. The reaction mixture was then cooled to room temperature and poured into a boiling mixture of water and EtOH (20 mL each). The mixture was stirred at rt for 1 h and then cooled (0-5° C.) overnight. EtOH was evaporated and the remainder of the mixture was diluted with water (100 mL). The obtained mixture was neutralized with Na2CO3 and extracted with EtOAc. The combined extract was washed with brine, dried with anhydrous MgSO4, filtered and evaporated. The residue was purified by chromatography on silica gel eluting with 5% MeOH in CH2Cl2, to afford 5.50 g (42%) of the title compound as a pink solid. 1H NMR (400 MHz, DMSO-d6) δ 9.25 (broad s, 1H), 7.05-7.40 (m, 4H), 2.55 (q, J=7.6 Hz, 2H), 2.02 (s, 3H), 1.09 (t, J=7.6 Hz, 3H).

Aufarbeitung

  1. temperatureThe reaction mixture was then cooled to room temperature
  2. temperaturecooled (0-5° C.) overnight
  3. customEtOH was evaporated
  4. additionthe remainder of the mixture was diluted with water (100 mL)
  5. extractionextracted with EtOAc
  6. extractionThe combined extract
  7. washwas washed with brine
  8. dry with materialdried with anhydrous MgSO4
  9. filtrationfiltered
  10. customevaporated
  11. customThe residue was purified by chromatography on silica gel eluting with 5% MeOH in CH2Cl2

Quellen und Nachweise

ORD-Eintrag
ord-e48dfc9e9e6646e1a23584973077f382
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09181276B2

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