Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cyclohexanone → Cyclohexene-1-yl acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cyclohexanone | HCID 7967 | — |
| 반응물 | 2-Nitrocyclohexanone | HCID 521241 | — |
| 생성물 | Cyclohexene-1-yl acetate | HCID 74019 | — |
반응 단계
nitrocyclohexanone process in which cyclohexanone is acetylated to obtain cyclohexenyl acetate, the obtained cyclohexenyl acetate is nitrated to obtain 2-nitrocyclohexanone, the obtained 2-nitrocyclohexanone is subjected to hydrolysis, thereby causing ring cleavage of the 2-nitrocyclohexanone to obtain nitrocapronic acid, the obtained nitrocapronic acid is hydrogenated to obtain ε-aminocapronic acid, and the obtained ε-aminocapronic acid is converted into ε-caprolactam.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06989444B2 |
| 출처 데이터셋 | uspto-grants-2006_01 |
| ORD ID | ord-ffbdc2a802f54936a47ccf1690561474 |
| 출처 메모 | uspto-grants-2006_01 |