Reaktion #89791

ord-8274997e6bfa423e9c35a065c31f784c

Reaktionsgleichung

NNc1cc(C(=O)O)cc(C(=O)O)c1
5-hydrazinylbenzene-1,3-dicarboxylic acid
CC(=O)C(C)C
isopropylmethylketone
CC1=Nc2cc(C(=O)O)cc(C(=O)O)c2C1(C)C
product
Ausbeute 95.5%
CC1=Nc2cc(C(=O)O)cc(C(=O)O)c2C1(C)C
2,3,3-Trimethyl-4,6-dicarboxy-3H-indole
Ausbeute 95.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux in an oil bath for 18 h
  2. 2
    Sonstigewas evaporated off under reduced pressure to a small volume of ˜100 mL
  3. 3
    workup.ADDITIONTo the crude mixture was added iPrOH (200 mL)
  4. 4
    Sonstigethe solid was collected with a filter funnel
  5. 5
    Waschenwashed with EtOAc (3×200 mL) and ethyl ether (2×200 mL)
  6. 6
    Sonstigedried
  7. 7
    SonstigeFurther drying of the solid in an oven at 50° C. under high vacuum for 18 h

Vorschrift

A solution of 5-hydrazinylbenzene-1,3-dicarboxylic acid (30.0 g, 129 mmol), isopropylmethylketone (22.0 mL, 205 mmol) in acetic acid (300 mL) and was heated under reflux in an oil bath for 18 h. After cooling to ambient temperature the solvent was evaporated off under reduced pressure to a small volume of ˜100 mL. To the crude mixture was added iPrOH (200 mL) and the solid was collected with a filter funnel, washed with EtOAc (3×200 mL) and ethyl ether (2×200 mL) and dried. Further drying of the solid in an oven at 50° C. under high vacuum for 18 h provided 30.44 g (95.5%) of the product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09441270B2uspto-grants-2016_09