Acetic Anhydride → N-[4-methyl-3-(2-phenoxy-ethoxy)-phenyl]-acetamide

HRID 330783Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 330783
[C:1](OC(=O)C)(=[O:3])[CH3:2].[NH2:8][C:9]1[CH:10]=[CH:11][C:12]([CH3:16])=[C:13]([OH:15])[CH:14]=1.Br[C:18]1[CH:19]=[C:20]([O:24][CH2:25][CH3:26])[CH:21]=[CH:22][CH:23]=1.C([O-])([O-])=O.[Cs+].[Cs+]>C(O)(=O)C.CN(C=O)C.O>[CH3:16][C:12]1[CH:11]=[CH:10][C:9]([NH:8][C:1](=[O:3])[CH3:2])=[CH:14][C:13]=1[O:15][CH2:26][CH2:25][O:24][C:20]1[CH:21]=[CH:22][CH:23]=[CH:18][CH:19]=1

Komponenten

8

Versuchsvorschrift

Acetic anhydride (1.25 mL, 12.2 mmol) was added to a solution of 5-amino-2-methyl phenol (1.0 g, 8.1 mmol) in acetic acid (6 mL), and the reaction was refluxed for 5 mins. Then the reaction mixture was cooled to room temperature and the product was solidified. It was filtered off and washed with water (4 mL) and dried to obtain the product along with the trace amount of O-acylated product. The mixture, to which was added 3-bromophenetole (1.33 g, 6.6 mmol) and Cs2CO3 (2.927 g, 9.0 mmol) in DMF (10 mL), was stirred overnight at 50° C. The reaction mixture was then diluted with water (10 mL) and extracted with ethyl acetate (3×20 mL). The combined extracts were dried over sodium sulfate and recrystallized from toluene to obtain the pure product 18a in 65% (yield over two steps) as an off-white solid.

Aufarbeitung

  1. temperaturethe reaction was refluxed for 5 mins
  2. filtrationIt was filtered off
  3. washwashed with water (4 mL)
  4. customdried
  5. customto obtain the product along with the trace amount of O-acylated product
  6. extractionextracted with ethyl acetate (3×20 mL)
  7. dry with materialThe combined extracts were dried over sodium sulfate
  8. customrecrystallized from toluene

Quellen und Nachweise

ORD-Eintrag
ord-904dd1e5c9634532a7bdbe92ef1dfa80
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08877752B2

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