HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl ((1-benzylpiperidin-4-yl)methyl)carbamate → Tert-butyl (piperidin-4-ylmethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl ((1-benzylpiperidin-4-yl)methyl)carbamate | HCID 2824066 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl (piperidin-4-ylmethyl)carbamate | HCID 723429 | 100% |
Reaction Steps
A solution of 1-benzyl-4-tertbutyloxycarbonylaminomethylpiperidine 8 (4.79 g; 15.7 mmol) in 120 ml of MeOH is poured into a hydrogenation reactor. The 10% Pd/C-based catalyst is added (0.872 g; 0.82 mmol) and the mixture is subjected to a hydrogen pressure of 3.5 bars (50 psi) for 24 hours in a Parr type shaker. After filtration on celite and washing with methanol, the medium is concentrated in order to produce 3.36 g (Yield=100%) of product in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745413B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-389f564054af4404af46e958b7bcb7da |
| Source note | uspto-grants-2010_06 |