Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164388Generated: October 26, 2026

Acetic Acid → Fomesafen

https://huagongshe.com/reaction/1164388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen PeroxideHCID 784—
ReactantNitric AcidHCID 944—
ReactantHCID 12799631HCID 12799631—
SolventWaterHCID 962—
ProductFomesafenHCID 51556—

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04369316
Source datasetuspto-grants-1983_01
ORD IDord-12889c89d49b4dbb9e6f10a14be5ec04
Source noteuspto-grants-1983_01