Toluene → 4-Amino-3-chloro-5-methoxyiminomethylbenzoyl chloride

HRID 363493

Reaktionsgleichung

Reaktionsgleichung von HRID 363493
[NH2:1][C:2]1[C:10]([CH:11]=[N:12][O:13][CH3:14])=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[Cl:15].C1(C)C=CC=CC=1.S(Cl)([Cl:25])=O>CN(C)C=O>[NH2:1][C:2]1[C:10]([CH:11]=[N:12][O:13][CH3:14])=[CH:9][C:5]([C:6]([Cl:25])=[O:7])=[CH:4][C:3]=1[Cl:15]

Komponenten

5

Edukt 3

HCID 1140TolueneHCID 24386Thionyl ChlorideHCID 540991344-Amino-3-chloro-5-methoxyiminomethylbenzoic acid

Produkt 1

HCID 544540514-Amino-3-chloro-5-methoxyiminomethylbenzoyl chloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

In a 5-liter three-necked round-bottomed flask was placed 180 g of the previously prepared 4-amino-3-chloro-5-methoxyiminomethylbenzoic acid, 2 l of toluene, 3 mL of dimethylformamide and 104 g (64 mL) of thionyl chloride. The resulting mixture was heated at 70° C. for 2 hours, filtered while hot and the solvent removed using a rotary evaporator yielding 178.1 g of the expected 4-amino-3-chloro-5-methoxyiminomethylbenzoyl chloride.

Aufarbeitung

  1. customIn a 5-liter three-necked round-bottomed flask was placed
  2. filtrationfiltered while hot and the solvent
  3. customremoved
  4. customa rotary evaporator

Quellen und Nachweise

ORD-Eintrag
ord-093d5ecf5a8647b684fe6f3e10bff9f9
Quelldatensatz
uspto-grants-1999_02
Patentnummer
US05874466

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