Reaktion #89790

ord-849145d5f1b84f94ad041af0e7fe6118

Reaktionsgleichung

NNc1cccc(C(=O)O)c1
3-hydrazinobenzoic acid
CC(=O)C(C)C
isopropylmethylketone
CC1=Nc2cccc(C(=O)O)c2C1(C)C
product
Ausbeute 81.4%
CC1=Nc2cccc(C(=O)O)c2C1(C)C
2,3,3-Trimethyl-4-carboxy-3H-indole
Ausbeute 81.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux in an oil bath for 20 h
  2. 2
    Sonstigewas evaporated off under reduced pressure to a small volume of ˜200 mL
  3. 3
    SonstigeCollected the solid with a filter funnel
  4. 4
    Waschenwashed with iPrOH (3×30 mL) and ethyl ether (3×30 mL)
  5. 5
    Sonstigedried
  6. 6
    SonstigeFurther drying of the solid in an oven at 45° C. under high vacuum for 18 h

Vorschrift

A solution of 3-hydrazinobenzoic acid (30.0 g, 197 mmol), isopropylmethylketone (31.7 mL, 296 mmol) in ethanol (500 mL) and sulfuric acid (5 mL) was heated under reflux in an oil bath for 20 h. After cooling to ambient temperature the solvent was evaporated off under reduced pressure to a small volume of ˜200 mL. Collected the solid with a filter funnel, washed with iPrOH (3×30 mL) and ethyl ether (3×30 mL) and dried. Further drying of the solid in an oven at 45° C. under high vacuum for 18 h provided 32.59 g (81.3%) of the product.

Quelle

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