HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate → 1-Boc-3-(aminomethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate | HCID 22647380 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Boc-3-(aminomethyl)piperidine | HCID 2756483 | 96% |
Reaction Steps
A mixture of 3-azidomethylpiperidine-1-carboxylic acid tert-butyl ester (5.0 g, 20.8 mmol), ethanol (125 mL) and 10% palladium on charcoal (1.5 g) was shaken under a hydrogen atmosphere (60 psig) for 5 hours. The mixture was filtered. The filtrate was concentrated to provide a colorless oil (4.27 g, 96%) which was used without further purification. 1H NMR (300 MHz, CDCl3) δ3.91 (b, 1H), 3.82 (dt, J=13, 4 Hz, 1H), 2.90 (m, 1H), 2.8-2.5 (m, 3H), 1.85 (m, 1H), 1.75 (s, 2H), 1.66 (m, 1H), 1.6-1.4 (m, 2H), 1.47 (s, 9H), 1.20 (m, 1H). Mass spec (AP+) m/z 215.2 (M+H+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919356B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-9545baed5c254b2cafc3c4a7c2ca9033 |
| Source note | uspto-grants-2005_07 |