HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-4-(N-tert-butoxycarbonyl-N-isopropylamino)piperidine → tert-butyl N-(piperidin-4-yl)-N-(propan-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-4-(N-tert-butoxycarbonyl-N-isopropylamino)piperidine | HCID 67428416 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-butyl N-(piperidin-4-yl)-N-(propan-2-yl)carbamate | HCID 50986573 | 99% |
Reaction Steps
A solution of 1-benzyl-4-(N-tert-butoxycarbonyl-N-isopropylamino)piperidine (79.0 g, 0.24 mol) in ethanol (140 mL) was flushed with nitrogen for 15 minutes. This solution was then added to a 2 L Parr flask containing a mixture of 10% palladium on carbon (15.8 g; ca. 50% wt. water) in ethanol (100 mL), which solution had been flushed with nitrogen for 15 minutes. This reaction mixture was placed on a Parr Shaker under hydrogen at 50 psi for 24 hours. The reaction mixture was filtered through a pad of Celite and the Celite washed with ethanol. The filtrate was then concentrated in vacuo to afford 57.0 g of the title intermediate as a white solid (>99% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285564B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-023f735e6bf5416ca0f2f4f3a198eb17 |
| Source note | uspto-grants-2007_10 |