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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1164388생성일: 2026년 10월 27일

Acetic Acid → Fomesafen

https://huagongshe.com/reaction/1164388

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrogen PeroxideHCID 784—
반응물Nitric AcidHCID 944—
반응물2-amino-5-(2-chloro-4-trifluoromethylphenoxy)-N-methanesulphonyl benzamideHCID 12799631—
용매WaterHCID 962—
생성물FomesafenHCID 51556—

반응 조건

온도70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04369316
출처 데이터셋uspto-grants-1983_01
ORD IDord-12889c89d49b4dbb9e6f10a14be5ec04
출처 메모uspto-grants-1983_01