Sulfuric Acid → 3-Chloro-5-nitrotoluene

HRID 1449584

Reaktionsgleichung

Reaktionsgleichung von HRID 1449584
[Cl:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[C:5]([N+:10]([O-:12])=[O:11])[C:3]=1N.S(=O)(=O)(O)O.N([O-])=O.[Na+]>C(O)C.O>[Cl:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[C:5]([N+:10]([O-:12])=[O:11])[CH:3]=1

Komponenten

6

Edukt 3

HCID 1118Sulfuric AcidHCID 795952-Chloro-6-nitro-p-toluidineHCID 23668193Sodium Nitrite

Produkt 1

HCID 2978873-Chloro-5-nitrotolueneAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

To a stirred mixture of 2-chloro-4-methyl-6-nitroaniline (7.39 g, 39.7 mM) and concentrated sulfuric acid (6.2 mL) in absolute ethanol (50 mL) at 0°-5° C. was slowly added a solution of sodium nitrite (6.85 g, 99.3 mM) in water (6 mL). The temperature of the reaction mixture was not allowed to exceed 5° C. during the addition. After the addition was completed, the reaction mixture was stirred at room temperature for 0.5 hr and then at reflux until the evolution of gas from the reaction mixture ceased. The reaction mixture was allowed to cool and was concentrated. The residue was slurried with ether and then filtered to remove the solids. The liltrate was concentrated and the residue chromatographed (eluant: diethyl ether/hexane; 1/9) to provide (6.25 g, 92%) the title compound as a yellow crystalline solid, mp 60.5°-61° C.; MS(CI): 172 (M+H).

Aufarbeitung

  1. additionto exceed 5° C. during the addition
  2. additionAfter the addition
  3. temperatureat reflux until the evolution of gas from the reaction mixture
  4. temperatureto cool
  5. concentrationwas concentrated
  6. filtrationfiltered
  7. customto remove the solids
  8. concentrationThe liltrate was concentrated
  9. customthe residue chromatographed (eluant: diethyl ether/hexane; 1/9)

Quellen und Nachweise

ORD-Eintrag
ord-7539af987af34130a84a27391cfb2a45
Quelldatensatz
uspto-grants-1997_02
Patentnummer
US05599814

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