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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128635생성일: 2026년 10월 26일

Cyproheptadine → 4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-methylpiperidine

https://huagongshe.com/reaction/128635

반응식

참여 물질

역할이름HCID투입량
반응물CyproheptadineHCID 2913—
반응물HCID 178418361HCID 178418361—
촉매Platinum oxide (PtO)HCID 82844—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
생성물4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-methylpiperidineHCID 16889794.2%

반응 단계

Dissolved cyproheptadine (22.2 g, 0.077 mol) in 150 mL of glacial acetic acid and 20 mL of ethanol. Added platinum oxide catalyst (1.0 g), and hydrogenated on Paar shaker at 57 psi of hydrogen pressure for 5 hours. Filtered, and evaporated filtrate to give a solid. Recrystallized crude product from ether-pet ether to give 21.0 g (94% yield) of 4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-methylpiperidine as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464840
출처 데이터셋uspto-grants-1995_11
ORD IDord-1683bda1f4484b42b484bd450eaf3c33
출처 메모uspto-grants-1995_11