돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219431생성일: 2026년 10월 26일

P-Anisidine → 3-Hydroxy-4'-methoxy-2-nitrobenzanilide

https://huagongshe.com/reaction/219431

반응식

참여 물질

역할이름HCID투입량
반응물P-AnisidineHCID 7732—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-Hydroxy-2-nitrobenzoic acidHCID 293291—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물3-Hydroxy-4'-methoxy-2-nitrobenzanilideHCID 1800113170.9%

반응 단계

3-Hydroxy-2-nitrobenzoic acid (1.83 g) was dissolved in 50 ml of N,N-dimethylformamide, then 1.23 g of 4-methoxyaniline, 2.50 g of 1-ethyl-3-dimethylaminopropylcarbodiimide hydrochloride, 1.35 g of 1-hydroxybenzotriazole and 1.81 ml of triethylamine were added and the mixture was stirred at room temperature for 66 hours. The reaction solution was concentrated in vacuo, water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated in vacuo. Chloroform was added to the resulting residue and the resulting precipitate was filtered to give 2.04 g of 3-hydroxy-4′-methoxy-2-nitrobenzanilide. The filtrate was purified by silica gel column chromatography using chloroform-methanol (98:2) as an eluting solvent, chloroform was added to the resulting crude product and the resulting precipitate was filtered to give additional 0.24 g of 3-hydroxy-4′-methoxy-2-nitrobenzanilide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE043481E1
출처 데이터셋uspto-grants-2012_06
ORD IDord-339d28b6bf48402cb347abd46101e9ab
출처 메모uspto-grants-2012_06