Potassium Nitrate → 5-nitro-1H-indazole-3-carboxylic Acid

HRID 1037999

Reaktionsgleichung

Reaktionsgleichung von HRID 1037999
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10]([OH:12])=[O:11])=[N:2]1.[N+:13]([O-])([O-:15])=[O:14].[K+]>S(=O)(=O)(O)O>[N+:13]([C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][N:2]=[C:3]2[C:10]([OH:12])=[O:11])([O-:15])=[O:14]

Komponenten

4

Edukt 2

HCID 24434Potassium NitrateHCID 78250Indazole-3-carboxylic acid2×

Produkt 1

HCID 71446525-nitro-1H-indazole-3-carboxylic AcidAusbeute 77,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1118Sulfuric AcidLösungsmittel

Versuchsvorschrift

To a suspension of indazole-3-carboxylic acid (compound 53, 3.0 g, 18 mmol) in 18 mL of concentrated sulfuric acid at 0 C was added potassium nitrate (2.0 g, 18 mmol). The reaction was stirred overnight at room temperature, poured into 150 mL of ice and extracted three times with ethyl acetate. The combined organic layer was washed with brine, dried and concentrated to give compound 54 (2.9 g) as the major isomer.

Aufarbeitung

  1. extractionextracted three times with ethyl acetate
  2. washThe combined organic layer was washed with brine
  3. customdried
  4. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-0a0fdad625654d2aac3086ba58f05015
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08546404B2

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