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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277420Erstellt: 25. Oktober 2026

Trifluoroacetic anhydride → 4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylaniline

https://huagongshe.com/reaction/277420

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic anhydrideHCID 9845—
EduktAmmonium nitrateHCID 22985—
EduktSodium BicarbonateHCID 516892—
Edukt4-chloro-2-fluoro-5-methyl-N-phenoxycarbonylanilineHCID 18615647—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
Produkt4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylanilineHCID 18615646103,1%

Reaktionsschritte

4-Chloro-2-fluoro-5-methyl-N-phenoxycarbonylaniline (7.1 g, 25.4 mmol) was dissolved in chloroform (68 ml) and trifluoroaceticanhydride (13.5 ml) and ammonium nitrate (2.4 g, 30.5 mmol) were slowly added with stirring at ambient temperature. The stirring was continued for 18 hr when a second batch of ammonium nitrate (0.4 g, 5 mmol) was added and stirring continued for 8 hr. Water was added and solution was neutralized by slow addition of sodium bicarbonate solution followed by extraction with chloroform. Organic layer was dried and evaporated under reduced pressure to afford an oily product (8.5 g) which was used for the next step without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355799B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-e79c080beabd48e5a7b746e48164ca14
Quellennotizuspto-grants-2002_03