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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249574Generated: October 29, 2026

3-[8-[4-(2,2-Diphenylethenyl)-1-piperidinyl]octyl]pyridine → 3-[8-[4-(2,2-Diphenylethyl)-1-piperidinyl]octyl]pyridine

https://huagongshe.com/reaction/1249574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[8-[4-(2,2-Diphenylethenyl)-1-piperidinyl]octyl]pyridineHCID 13754506—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-[8-[4-(2,2-Diphenylethyl)-1-piperidinyl]octyl]pyridineHCID 1375454782%

Reaction Steps

The title compound was prepared by the hydrogenation of 7.3 g of 3-[8-[4-(2,2-diphenylethenyl)-1-piperidinyl]octyl]pyridine at ambient conditions using 100 mL of ethanol and 1.5 g of 10% palladium on carbon catalyst. After filtration and evaporation, the residue was crystallized from hexane to give 6.0 g (82%) of 3-[8-[4-(2,2-diphenylethyl)-1-piperidinyl]octyl]pyridine, mp 68°-70° C. Analysis Calculated for C32H42N2 : C, 84.53: H, 9.31; N, 6.16. Found: C, 84.68; H, 9.15; N, 6.12. The fumarate salt was crystallized from acetone, mp 110°-111° C. Analysis Calculated for C32H42N2.C4H4O4 : C, 75.76; H, 8.12; N, 4.91. Found: C, 75.59; H, 8.00; N, 4.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632925
Source datasetuspto-grants-1986_12
ORD IDord-fc5f4f1e7b6042e3906235a1cd558539
Source noteuspto-grants-1986_12