돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 597246생성일: 2026년 10월 26일

Benzene → (Z)-2-cyclohexanecarbonyl-1,2,3,4-tetrahydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]isoquinoline

https://huagongshe.com/reaction/597246

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물Cyclohexanecarbonyl chlorideHCID 75938—
반응물3,4-Dihydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]isoquinolineHCID 70638952—
용매PyridineHCID 1049—
생성물(Z)-2-cyclohexanecarbonyl-1,2,3,4-tetrahydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]isoquinolineHCID 68123591—

반응 단계

To a suspension of 5 parts of 3,4-dihydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]isoquinoline in 50 parts of benzene is added 15 parts of pyridine, followed by 3 parts of cyclohexanecarbonyl chloride. The resultant mixture is heated at the boiling point under reflux in a nitrogen atmosphere for 2 hours, then cooled, consecutively washed with water and aqueous 5% sodium becarbonate, dried over anhydrous sodium sulfate, and stripped of solvent by vacuum distillation. The residue is crystallized from a mixture of ethyl acetate and ether to afford (Z)-2-cyclohexanecarbonyl-1,2,3,4-tetrahydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]isoquinoline melting at 162°-164°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04013666
출처 데이터셋uspto-grants-1977_03
ORD IDord-81438d8ec2ac4a6aab9449b93115f1d3
출처 메모uspto-grants-1977_03