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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230707Erstellt: 24. Oktober 2026

Nitric Acid → Ethanone, 1-(5-amino-2-nitrophenyl)-

https://huagongshe.com/de/reaction/230707

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
EduktAmmonium HydroxideHCID 14923—
EduktAcetanilide, 3'-acetyl-2,2,2-trifluoro-HCID 673706—
LösungsmittelSulfuric AcidHCID 1118—
ProduktEthanone, 1-(5-amino-2-nitrophenyl)-HCID 642038654%

Reaktionsschritte

10 mmol of 3-acetyl-trifluoroacetylaminobenzene as a starting material was slowly added dropwise to 20 mL of concentrated H2SO4 at −20° C. and the reaction mixture was stirred 30 minutes. Then, nitric acid was slowly added dropwise thereto over 10 minutes. The reaction mixture was continuously stirred for 2 hours. When the reaction was completed, ice water was poured into the reaction mixture. The reaction mixture was extracted twice with 50 mL of ethyl acetate. The organic layer was washed with a solution of sodium hydrogen carbonate and dried over anhydrous sodium sulfate. The ethyl acetate was then distilled off under reduced pressure to give an impure product. The impure produce was added to concentrated NH4OH and stirred at 50° C. for 1 hour. The reaction mixture was evaporated on a rotary evaporator and extracted with EtOAc and water, and purified by silica gel column chromatography (hexane/EtOAc=3/1) to obtain the desired 3-acetyl-4-nitro-aminobenzene as a brown solid (54%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07566773B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-599429a758dc4130918100e567fb92ec
Quellennotizuspto-grants-2009_07