Reaktion #4177

ord-a49a0ffb48db4738a1beaed2e1be1dd6

Reaktionsgleichung

[K+].[OH-]
potassium hydroxide
OCCO
ethylene glycol
Cc1cc2c(c([N+](=O)[O-])c1)N(c1ccccc1C#N)CC2
2-(5-methyl-7-nitroindolin-1-yl)benzonitrile
ClCCl
dichloromethane
Cc1cc2c(c([N+](=O)[O-])c1)N(c1ccccc1C(=O)O)CC2
product
Ausbeute 32.0%
Cc1cc2c(c([N+](=O)[O-])c1)N(c1ccccc1C(=O)O)CC2
2-(5-Methyl-7-nitro-1-indolinyl)benzoic acid
Ausbeute 32.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
175°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction mixture was cooled to room temperature
  2. 2
    SonstigeThe aqueous phase was separated
  3. 3
    Extraktionextracted with two 250 ml-portions of dichloromethane
  4. 4
    TemperaturThe aqueous phase was then cooled in an ice-bath
  5. 5
    ExtraktionThe product was extracted out with three 500 ml-portions of dichloromethane
  6. 6
    WaschenThe combined organic extracts were washed twice with brine
  7. 7
    Sonstigedried
  8. 8
    Filtrationfiltered
  9. 9
    Einengenconcentrated

Vorschrift

A stirred solution under nitrogen of potassium hydroxide (30 g, 0.53 mole) in ethylene glycol (250 ml) and water (35 ml) was heated to 175° C., at which temperature there was added 2-(5-methyl-7-nitroindolin-1-yl)benzonitrile (26 g, 0.093 mole). After heating at 175° C. for 3 hours, the reaction mixture was cooled to room temperature and dichloromethane (1 liter) and water (500 ml), were added, with stirring. The aqueous phase was separated and extracted with two 250 ml-portions of dichloromethane. The aqueous phase was then cooled in an ice-bath and acidified with concentrated hydrochloric acid. The product was extracted out with three 500 ml-portions of dichloromethane. The combined organic extracts were washed twice with brine, dried, filtered, and concentrated to afford 9.0 g (32%) of product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723003uspto-grants-1988_02