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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2421생성일: 2026년 10월 23일

4-Nitrobenzoic Acid → N-(2-methoxyphenyl)-4-nitrobenzamide

https://huagongshe.com/ko/reaction/2421

반응식

참여 물질

역할이름HCID투입량
반응물4-Nitrobenzoic AcidHCID 6108—
반응물2-MethoxyanilineHCID 7000—
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DichloromethaneHCID 6344—
생성물N-(2-methoxyphenyl)-4-nitrobenzamideHCID 77451387.5%

반응 단계

With cooling in an ice bath, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC.HCl) (630 mg, 3.29 mmol) was added to 15 ml of methylene chloride solution containing o-anisidine (368 mg, 2.99 mmol) and 4-nitrobenzoic acid (500 mg, 2.99 mmol). After 1 hour of stirring at the same temperature, the reaction mixture was roughly adjusted to pH 8 with saturated sodium bicarbonate aqueous solution, extracted with methylene chloride and then washed with water and saturated brine in that order. After drying on anhydrous magnesium sulfate, the solvent was removed by evaporation, and the resulting solid material was purified by silica gel column chromatography (methylene chloride) to obtain 712 mg (87.4%) of the title compound in the form of yellow powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728835
출처 데이터셋uspto-grants-1998_03
ORD IDord-c4ba4a81e15b4995a5093c01878efc4c
출처 메모uspto-grants-1998_03