HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 4-(4-chlorobenzylidene)piperidine-1-carboxylate → Tert-butyl 4-(4-chlorobenzyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 4-(4-chlorobenzylidene)piperidine-1-carboxylate | HCID 22893850 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tert-butyl 4-(4-chlorobenzyl)piperidine-1-carboxylate | HCID 22893851 | 99.3% |
Reaction Steps
A solution of 2 g of 4-(4-chloro-benzylidene)-piperidine-1-carboxylic acid tert-butyl ester and 0.5 g of 5% platinum on carbon in 10 mL of ethanol was allowed to stir overnight under 1 atm of hydrogen. The catalyst was filtered off and, the solution concentrated to give 2 g of 4-(4-chloro-benzyl)-piperidine-1-carboxylic acid tert-butyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06476041B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-4e1c8dc359394203ba0dae17b6a8ba8b |
| Source note | uspto-grants-2002_11 |