돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1611721생성일: 2026년 10월 24일

Cyclohexanone → Cyclohexene-1-yl acetate

https://huagongshe.com/ko/reaction/1611721

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanoneHCID 7967—
반응물2-NitrocyclohexanoneHCID 521241—
생성물Cyclohexene-1-yl acetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06989444B2
출처 데이터셋uspto-grants-2006_01
ORD IDord-ffbdc2a802f54936a47ccf1690561474
출처 메모uspto-grants-2006_01