p-Nitroacetophenone → 3-(4-Nitrophenyl)-1H-pyrazole

HRID 1180873

Reaktionsgleichung

Reaktionsgleichung von HRID 1180873
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=O)[CH3:11])=[CH:6][CH:5]=1)([O-:3])=[O:2].CO[CH:15](OC)[NH2:16].O.[NH2:20]N>CN(C)C=O>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[NH:20][N:16]=[CH:15][CH:11]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2]

Komponenten

5

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

A solution of 1-(4-nitrophenyl)ethanone (605.5 mmol) and bis(methyloxy)methanamine (726 mmol) in N,N-dimethylformamide (1000 mL) was stirred for 1 h at 80° C. The reaction was concentrated in vacuo, the residue was dissolved in ethanol (1000 mL) and treated with hydrazine monohydrate (1816 mmol). After the reaction stirred 2 h at 70° C. it was cooled to room temperature and poured into ice-water (2000 mL). Product precipitated out of solution, which was filtered, washed with water (4×500 mL) and dried to provide the title product as a yellow powder (98%). ESMS [M+H]+: 190.2

Aufarbeitung

  1. concentrationThe reaction was concentrated in vacuo
  2. dissolutionthe residue was dissolved in ethanol (1000 mL)
  3. temperaturewas cooled to room temperature
  4. customProduct precipitated out of solution, which
  5. filtrationwas filtered
  6. washwashed with water (4×500 mL)
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-2fa60280d70240f690012016dd022521
Quelldatensatz
uspto-grants-2007_10
Patentnummer
US07282588B2

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