Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → N-phenyl-5-nitro-2-thienylamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Thiophene, 2-nitro- | HCID 11866 | — |
| 반응물 | Benzenesulfenamide, N-phenyl- | HCID 315504 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-phenyl-2-nitro-3-thienylamine | HCID 13039998 | 15% |
| 생성물 | N-phenyl-5-nitro-2-thienylamine | HCID 19783600 | 42% |
반응 단계
2.9 g of 2-nitrothiophene and 4 g of N-phenylbenzenesulphenamide, dissolved in 10 ml of dimethylformamide, are added dropwise to a stirred solution of 6 g of potassium tert.-butylate in 60 ml of dimethylformamide, while the temperature is kept at about -20° C. The mixture is stirred for a further 15 minutes; then an excess of dilute hydrochloric acid is added to the mixture, after which it is treated in the same way as described in Example 1. The crude product is separated by column chromatography; N-phenyl-5-nitro-2-thienylamine (melting point 186° C., yield 1.8 g, 42%) and N-phenyl-2-nitro-3-thienylamine (melting point 105° C., yield 0.7 g, 15%) are obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05262539 |
| 출처 데이터셋 | uspto-grants-1993_11 |
| ORD ID | ord-163f67be382447bcb75b33046858f377 |
| 출처 메모 | uspto-grants-1993_11 |