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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1164388Erstellt: 26. Oktober 2026

Acetic Acid → Fomesafen

https://huagongshe.com/reaction/1164388

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrogen PeroxideHCID 784—
EduktNitric AcidHCID 944—
Edukt2-amino-5-(2-chloro-4-trifluoromethylphenoxy)-N-methanesulphonyl benzamideHCID 12799631—
LösungsmittelWaterHCID 962—
ProduktFomesafenHCID 51556—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A stirred solution is prepared containing 39.5 g of 2-amino-5-(2-chloro-4-trifluoromethylphenoxy)-N-methanesulphonyl benzamide of the formula (V), R1 =methyl, 1380 ml of glacial acetic acid and 1.0 g of concentrated nitric acid at about 40° C. To the solution is added 138 g of a 30% by weight hydrogen peroxide in water solution and the reaction mixture is raised to and maintained at about 70° C. for 20 hours. The solution is then poured slowly into about 3 liters of ice water with precipitation of crude product. After filtration, the product is isolated as a solid, m.p. 175°-183° C., containing 68% of the compound of formula (I), R1 =methyl, as determined by high pressure liquid chromatography, thin layer chromatography and its mass spectrum. Recrystallization from aqueous methanol yields the product 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitro-N-methanesulphonyl benzamide, m.p. 216°-218° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04369316
Quelldatensatzuspto-grants-1983_01
ORD IDord-12889c89d49b4dbb9e6f10a14be5ec04
Quellennotizuspto-grants-1983_01