HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Cbz-aminopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Boc-4-Cbz-amino-piperidine | HCID 1514305 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Cbz-aminopiperidine | HCID 1514304 | 99.1% |
Reaction Steps
A mixture of tert-butyl 4-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylate obtained in Example 1a (13.1 g, 39.2 mmol), a 5 N aqueous hydrochloric acid solution (40 ml, 200 mmol) and methanol (40 ml) was stirred at mom temperature for 23 hours. A 5 N aqueous sodium hydroxide solution (40 ml) was added to the reaction mixture under ice-cooling. Water and the solvent were distilled off from the reaction mixture while the mixture was azeotropically distilled with ethanol. Ethanol was added to the residue, the insoluble matter was removed by filtration, and the filtrate was concentrated to give the title compound (9.10 g, yield 99.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476301B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-d8a9c155dc574bdb9a6e6b801bbdf0b2 |
| Source note | uspto-grants-2013_07 |