Dimethyl Sulfate → 4-Methoxy-N-methyl-3-nitrobenzeneacetamide

HRID 975927Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 975927
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([NH:11][CH3:12])=[O:10])=[CH:4][C:3]=1[N+:13]([O-:15])=[O:14].[C:16](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O.S([O-])(OC)(=O)=O>CN(C=O)C.O>[CH3:16][O:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([NH:11][CH3:12])=[O:10])=[CH:4][C:3]=1[N+:13]([O-:15])=[O:14]

Komponenten

7

Versuchsvorschrift

To a solution of 4.2 g (19.8 mmol) of 4-hydroxy-N-methyl-3 -nitrobenzeneacetamide in 50 mL of DMF containing 5.5 g of anhydrous potassium carbonate was added 5.6 mL of dimethyl sulfate. The mixture was heated at 60°-70° C. for 45 min, treated with an additional 3.0 mL of methyl sulfate, and heated for another 30 min. The mixture was cooled, poured into 200 mL water, and extracted with dichloromethane. The extracts were washed with water, dried and evaporated to give a solid which was recrystallized from ethanol-water to afford 3.7 g of a yellowish solid (82%). 1H NMR (300 MHz, CDCl3) δ 7.71 (s, 1H), 7.47 (d, 1H, J =9.0 Hz), 7.25 (d, 1H, J =8.4 Hz), 5.71 (brs, 1H), 3.90 (s, 3H) 3.47 (s, 2H), 2.75 (d, 3H, J=4.8 Hz).

Aufarbeitung

  1. temperatureThe mixture was heated at 60°-70° C. for 45 min
  2. temperatureheated for another 30 min
  3. temperatureThe mixture was cooled
  4. extractionextracted with dichloromethane
  5. washThe extracts were washed with water
  6. customdried
  7. customevaporated
  8. customto give a solid which
  9. customwas recrystallized from ethanol-water

Quellen und Nachweise

ORD-Eintrag
ord-9296010060b6485aba8463c6a3b5e3eb
Quelldatensatz
uspto-grants-1997_03
Patentnummer
US05610174

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