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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484785생성일: 2026년 10월 24일

2-Methyl-4-nitroaniline → N-(2-Methyl-4-nitrophenyl)-3,4-dihydro-2H-pyrrol-5-amine

https://huagongshe.com/ko/reaction/484785

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-4-nitroanilineHCID 7441—
반응물2-Chloro-1-pyrrolineHCID 13520141—
용매AcetonitrileHCID 6342—
생성물N-(2-Methyl-4-nitrophenyl)-3,4-dihydro-2H-pyrrol-5-amineHCID 1352014251.5%

반응 단계

A mixture of 2-chloro-1-pyrroline (1.2 mole), prepared as in Example 1, and 91.3 g (0.6 mole) of 2-methyl-4-nitroaniline were heated at reflux in 900 ml of acetonitrile for two hours. The solid obtained by cooling and filtering was combined with that obtained by concentrating the filtrate to dryness, then dissolved in hot water and filtered. The solution was cooled and washed with ethyl acetate, and the aqueous phase was made basic with 4 N sodium hydroxide. The crude product was extracted into dichloromethane, which was then removed in vacuo. The resultant solid was washed repeatedly with diethyl ether to give 67.7 g of pure title compound. Structure assignment was supported by the nmr spectrum and by elemental analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04533739
출처 데이터셋uspto-grants-1985_08
ORD IDord-51e1a3db10db46469f4db076b15c57ae
출처 메모uspto-grants-1985_08