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HRID 581950생성일: 2026년 10월 24일

N-(4-bromo-2-nitrophenyl)acetamide → N-Acetyl 4-(3-furanyl)-2-nitroaniline

https://huagongshe.com/ko/reaction/581950

반응식

참여 물질

역할이름HCID투입량
반응물N-(4-bromo-2-nitrophenyl)acetamideHCID 136690—
반응물Sodium BicarbonateHCID 516892—
반응물Furan-3-boronic acidHCID 2734358—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-Acetyl 4-(3-furanyl)-2-nitroanilineHCID 5409475676%

반응 조건

온도80 °C

반응 단계

A mixture of 1d from Example 18 (8.5 g, 32.8 mmol), 3-furanylboronic acid (3.67 g, 32.8 mmol), sodium bicarbonate (13.8 g, 0.16 mol) and tetrakis(triphenylphosphine)palladium(0) (0.5 g) in a mixture of water (40 ml) and dimethoxyethane (80 ml) is heated to 80° C. under a stream of nitrogen over night. After cooling the mixture is poured into water and extracted with ethyl acetate. The organic phase is washed with brine, dried over sodium sulfate and concentrated under reduced pressure.(*). The residue is dissolved in 40 ml dimethoxyethane. Aqueous sodium hydroxide (78 ml, 1 M) is added and the mixture is stirred at ambient temperature over night. The mixture is poured into water and rendered acidic with diluted hydrochloric acid. The precipitate is filtered off, washed with water and dried to yield 1e (5.09 g, 76%). Mp 152-154° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05922724
출처 데이터셋uspto-grants-1999_07
ORD IDord-3e5b9130d7dd4c5483cca17b90d6c1eb
출처 메모uspto-grants-1999_07