Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Trifluoroacetic anhydride → 4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylaniline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Trifluoroacetic anhydride | HCID 9845 | — |
| 반응물 | Ammonium nitrate | HCID 22985 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 4-chloro-2-fluoro-5-methyl-N-phenoxycarbonylaniline | HCID 18615647 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylaniline | HCID 18615646 | 103.1% |
반응 단계
4-Chloro-2-fluoro-5-methyl-N-phenoxycarbonylaniline (7.1 g, 25.4 mmol) was dissolved in chloroform (68 ml) and trifluoroaceticanhydride (13.5 ml) and ammonium nitrate (2.4 g, 30.5 mmol) were slowly added with stirring at ambient temperature. The stirring was continued for 18 hr when a second batch of ammonium nitrate (0.4 g, 5 mmol) was added and stirring continued for 8 hr. Water was added and solution was neutralized by slow addition of sodium bicarbonate solution followed by extraction with chloroform. Organic layer was dried and evaporated under reduced pressure to afford an oily product (8.5 g) which was used for the next step without purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06545161B2 |
| 출처 데이터셋 | uspto-grants-2003_04 |
| ORD ID | ord-4741a347fe21462983bdea91d7fc2dad |
| 출처 메모 | uspto-grants-2003_04 |