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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230707생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/230707

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Ammonium HydroxideHCID 14923—
반응물Acetanilide, 3'-acetyl-2,2,2-trifluoro-HCID 673706—
용매Sulfuric AcidHCID 1118—
생성물Ethanone, 1-(5-amino-2-nitrophenyl)-HCID 642038654%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566773B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-599429a758dc4130918100e567fb92ec
출처 메모uspto-grants-2009_07