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HRID 230707作成日:2026年10月26日

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

https://huagongshe.com/reaction/230707

反応式

関与物質

役割名称HCID仕込み量
反応物Nitric AcidHCID 944—
反応物Ammonium HydroxideHCID 14923—
反応物Acetanilide, 3'-acetyl-2,2,2-trifluoro-HCID 673706—
溶媒Sulfuric AcidHCID 1118—
生成物Ethanone, 1-(5-amino-2-nitrophenyl)-HCID 642038654%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566773B2
出典データセットuspto-grants-2009_07
ORD IDord-599429a758dc4130918100e567fb92ec
出典メモuspto-grants-2009_07