HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-Tert-butyloxycarbonyl-4-(4-amino-3-methylphenyloxy)piperidine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-butyl 4-(3-methyl-4-nitrophenoxy)piperidine-1-carboxylate | HCID 18542679 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Tert-butyloxycarbonyl-4-(4-amino-3-methylphenyloxy)piperidine hydrochloride | HCID 23366892 | — |
Reaction Steps
To a solution of 1-tert-butyloxycarbonyl-4-(4-nitro-3-methylphenyloxy)piperidine (3.6 g) in ethanol (30 ml) was added conc. hydrochloric acid (0.9 ml). By using 10% palladium/carbon (containing 48% water, 0.3 g) as a catalyst, catalytic reduction was conducted under reduced pressure for 1.5 hours. The catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to obtain 1-tert-butyloxycarbonyl-4-(4-amino-3methylphenyloxy)piperidine hydrochloride (1.7 g) as light brown crystals, m.p. 160°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580883 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-e84e5074125b47359766b579fcc246ce |
| Source note | uspto-grants-1996_12 |