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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128638생성일: 2026년 10월 26일

4-[10,11-dihydro-5-(2-propenyl)-5H-dibenzo[a,d]cyclohepten-5-yl]-1-methyl-1,2,5,6-tetrahydropyridine → 4-[10,11-dihydro-5-propyl-5H-dibenzo[a,d]cyclohepten-5-yl]-1-methylpiperidine

https://huagongshe.com/reaction/128638

반응식

참여 물질

역할이름HCID투입량
반응물4-[10,11-dihydro-5-(2-propenyl)-5H-dibenzo[a,d]cyclohepten-5-yl]-1-methyl-1,2,5,6-tetrahydropyridineHCID 9797563—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물4-[10,11-dihydro-5-propyl-5H-dibenzo[a,d]cyclohepten-5-yl]-1-methylpiperidineHCID 214741288%

반응 단계

Dissolved 4-[10,11-dihydro-5-(2-propenyl)-5H-dibenzo[a,d]cyclohepten-5-yl]-1-methyl-1,2,5,6-tetrahydropyridine (0.33 g, 1.0 mmol) in 50 mL of absolute ethanol, and added 0.15 g of 10% palladium on carbon catalyst. Hydrogenated on a Paar shaker at 60 psi of hydrogen pressure for 24 hours. Filtered catalyst, and evaporated filtrate. Crystallized product from dichloromethane-ether to give 26 mg (8% yield) of 4-[10,11-dihydro-5-propyl-5H-dibenzo[a,d]cyclohepten-5-yl]-1-methylpiperidine as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464840
출처 데이터셋uspto-grants-1995_11
ORD IDord-f34829a7205d4d42bfa01e6b2b1d2955
출처 메모uspto-grants-1995_11