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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128635Generated: October 25, 2026

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

https://huagongshe.com/reaction/128635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyproheptadineHCID 2913—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-methylpiperidineHCID 16889794.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464840
Source datasetuspto-grants-1995_11
ORD IDord-1683bda1f4484b42b484bd450eaf3c33
Source noteuspto-grants-1995_11