Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → Benzenamine, 4-chloro-N-ethyl-2-nitro-
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Acetaldehyde | HCID 177 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | 4-Chloro-2-nitroaniline | HCID 6979 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Ethyl acetate hexane | HCID 21226206 | — |
| 생성물 | Benzenamine, 4-chloro-N-ethyl-2-nitro- | HCID 97006 | 50% |
반응 단계
4-chloro-2-nitroaniline (8.6 g; 0.05 mole), acetaldehyde (5.5 ml; 0.05 mole) and HOAc (4.0 ml; 0.1 moles) were dissolved in toluene (100 ml) and stirred for 1 hr. BH3 * pyridine (5.0 ml; 0.01 moles) was added in 1.0 ml increments. The reaction was exothermic, and the reaction progress was monitored by tlc (40%EtOAc/Hexane). Additional TFA, BH3 * pyridine and acetaldehyde were added until the tlc indicated that the 4-chloro-2-nitroaniline was consumed. The reaction mixture was washed 2X with water and placed on a bed of silica and eluted with 20% EtOAc/Hexane. The product was the first major component to elute. The product was crystallized from MeOH which produced 5.0 g (50%) of a yellow crystalline solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05521193 |
| 출처 데이터셋 | uspto-grants-1996_05 |
| ORD ID | ord-730cd785fd4d49a6a6507551a1e20aeb |
| 출처 메모 | uspto-grants-1996_05 |