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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129082Generated: October 28, 2026

1-(4-Chlorobenzoyl)-4-(4-cyanobenzylidene)piperidine → 1-(4-Chlorobenzoyl)-4-(4-cyanobenzyl)piperidine

https://huagongshe.com/reaction/129082

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Chlorobenzoyl)-4-(4-cyanobenzylidene)piperidineHCID 15231398—
CatalystPalladiumHCID 23938—
SolventTolueneHCID 1140—
Product1-(4-Chlorobenzoyl)-4-(4-cyanobenzyl)piperidineHCID 19372710—

Reaction Steps

8.4 g of 1-(4-chlorobenzoyl)-4-(4-cyanobenzylidene)piperidine are hydrogenated (5 bar) at ambient temperature for 15 minutes in 400 ml of toluene with the addition of 2 g of palladium black. After addition of 1 g of palladium black, the mixture is hydrogenated for an additional 2.5 hours, a further 1 g of catalyst is added and the mixture is hydrogenated for an additional hour. 7.9 g (93.3% of theory) of the title compound are obtained as a colourless powder of melting point 137°-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466687
Source datasetuspto-grants-1995_11
ORD IDord-a74b541a920247af92da80551b4f1739
Source noteuspto-grants-1995_11