Sulfuric Acid → 2-Amino-4,6-Dinitrotoluene

HRID 1283963

Reaktionsgleichung

Reaktionsgleichung von HRID 1283963
OS(O)(=O)=O.O=S(=O)=O.S(=O)(=O)(O)O.[N+:15]([C:18]1[C:19]([CH3:30])=[C:20]([CH:24]=[C:25]([N+:27]([O-:29])=[O:28])[CH:26]=1)C(O)=O)([O-:17])=[O:16].[N-:31]=[N+]=[N-].[Na+]>C(OCC)(=O)C.C(Cl)(Cl)Cl>[N+:15]([C:18]1[C:19]([CH3:30])=[C:20]([CH:24]=[C:25]([N+:27]([O-:29])=[O:28])[CH:26]=1)[NH2:31])([O-:17])=[O:16]

Komponenten

7

Edukt 4

HCID 1118Sulfuric AcidHCID 24681Fuming sulfuric acidHCID 33557Sodium AzideHCID 988242-Methyl-3,5-dinitrobenzoic acid

Produkt 1

HCID 371822-Amino-4,6-DinitrotolueneAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6212ChloroformLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
45 °C

Versuchsvorschrift

Chloroform (38 ml.) was added carefully to a stirred mixture of oleum (16.9 ml.: 20% free sulphur trioxide) and concentrated sulphuric acid (3.8 ml.) followed by 3,5-dinitro-2-methylbenzoic acid (10.0 g.). The mixture was warmed to 45°C. and sodium azide (3.28 g.) was added in small portions over 20 minutes, the temperature of the reaction mixture being kept between 45° and 50°C. by means of intermittent cooling. After the addition was complete, the mixture was stirred and heated under reflux for 1 hour on the steam bath and then the chloroform was removed by decantation and the residue was poured into ice-water (300 ml.). The yellow precipitate was filtered off, washed with water and dried, to give crude 3,5-dinitro-2-methylaniline (8.8 g.), m.p. 169°-171°C. The crude product was dissolved in ethyl acetate, washed with saturated aqueous sodium bicarbonate solution and then with water and the solvent was removed in vacuo. Trituration with petroleum ether (b.p. 40°-60°C.) gave 3,5-dinitro-2-methylaniline (7.5 g.), m.p. 172.5°-174.5°C.

Aufarbeitung

  1. custombeing kept between 45° and 50°C. by means of intermittent cooling
  2. additionAfter the addition
  3. temperatureheated
  4. temperatureunder reflux for 1 hour on the steam bath
  5. customthe chloroform was removed by decantation
  6. additionthe residue was poured into ice-water (300 ml.)
  7. filtrationThe yellow precipitate was filtered off
  8. washwashed with water
  9. customdried
  10. customto give crude 3,5-dinitro-2-methylaniline (8.8 g.), m.p. 169°-171°C
  11. washwashed with saturated aqueous sodium bicarbonate solution
  12. customwith water and the solvent was removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-adc07a7c285c4fa1a5e7516989145b0f
Quelldatensatz
uspto-grants-1976_08
Patentnummer
US03976786

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