Reaktion #522785

ord-c4ecc46c4d864aa497e4019124e8deab

Reaktionsgleichung

O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulphate
Cc1ccc(N)c(C(=O)O)c1
5-methyl-anthranilic acid
[I-].[K+]
potassium iodide
Cl
hydrochloric acid
O=N[O-].[Na+]
sodium nitrite
Cl
hydrochloric acid
Cc1ccc(I)c(C(=O)O)c1
2-iodo-5-methyl-benzoic acid

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONThere is added dropwise
  2. 2
    workup.STIRRINGThe mixture is then stirred for a further 30 minutes at room temperature and for 2 hours
  3. 3
    Temperaturunder reflux
  4. 4
    TemperaturThe mixture is then cooled

Vorschrift

20 g of 5-methyl-anthranilic acid are suspended in 200 ml of 3-N hydrochloric acid at 0° C. There is added dropwise thereto with stirring a solution of 10 g of sodium nitrite and 20 ml of water and the mixture is stirred for 25 minutes at 0° C. A solution of 26.5 g of potassium iodide, 30 ml of 3-N hydrochloric acid and 30 ml of water is then added dropwise at 5°-10° C. The mixture is then stirred for a further 30 minutes at room temperature and for 2 hours under reflux. The mixture is then cooled, sodium thiosulphate is added until the solution is yellow (5 g) and the crystalline 2-iodo-5-methyl-benzoic acid obtained is filtered under suction and washed with water until neutral. The crude acid is dissolved in ether, washed well with sodium thiosulphate solution and water, dried over sodium sulphate and evaporated. There are obtained light-brown crystals of melting point 100°-112° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04006145uspto-grants-1977_02