HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Chlorobenzoyl)-4-(4-cyanobenzylidene)piperidine → 1-(4-Chlorobenzoyl)-4-(4-cyanobenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Chlorobenzoyl)-4-(4-cyanobenzylidene)piperidine | HCID 15231398 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-Chlorobenzoyl)-4-(4-cyanobenzyl)piperidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466687 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-a74b541a920247af92da80551b4f1739 |
| Source note | uspto-grants-1995_11 |