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

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%).

1. waitover 10 minutes
2. stirringThe reaction mixture was continuously stirred for 2 hours
3. extractionThe reaction mixture was extracted twice with 50 mL of ethyl acetate
4. washThe organic layer was washed with a solution of sodium hydrogen carbonate
5. dry with materialdried over anhydrous sodium sulfate
6. distillationThe ethyl acetate was then distilled off under reduced pressure
7. customto give an impure product
8. customThe impure produce
9. stirringstirred at 50° C. for 1 hour
10. customThe reaction mixture was evaporated on a rotary evaporator
11. extractionextracted with EtOAc and water
12. custompurified by silica gel column chromatography (hexane/EtOAc=3/1)

ORD 기록

ord-599429a758dc4130918100e567fb92ec

출처 데이터셋

uspto-grants-2009_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07566773B2