Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Methyl-4-nitroaniline → N-(2-Methyl-4-nitrophenyl)-3,4-dihydro-2H-pyrrol-5-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Methyl-4-nitroaniline | HCID 7441 | — |
| 반응물 | 2-Chloro-1-pyrroline | HCID 13520141 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-(2-Methyl-4-nitrophenyl)-3,4-dihydro-2H-pyrrol-5-amine | HCID 13520142 | 51.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04533739 |
| 출처 데이터셋 | uspto-grants-1985_08 |
| ORD ID | ord-51e1a3db10db46469f4db076b15c57ae |
| 출처 메모 | uspto-grants-1985_08 |