HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → tert-Butyl 4-(aminooxy)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Tert-butyl 4-(1,3-dioxoisoindolin-2-yloxy)piperidine-1-carboxylate | HCID 21751544 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 4-(aminooxy)piperidine-1-carboxylate | HCID 24729482 | 88% |
Reaction Steps
Hydrazine solution (1.40 g, 29.0 mmol) was added to a solution of tert-butyl 4-(1,3-dioxoisoindolin-2-yloxy)piperidine-1-carboxylate (5.00 g, 14.5 mmol) in ethanol (50 ml) and stirred at room temperature for 30 minutes. The resulting solid was filtered off and the filtrate was concentrated in vacuo. The residue was triturated with diethyl ether (30 ml), and the resulting solid was filtered off again and concentrated in vacuo to give tert-butyl 4-(aminooxy)piperidine-1-carboxylate (2.75 g, 88%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518934B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-dd6393b58ca6440cba90dc0bf4b8bfdd |
| Source note | uspto-grants-2013_08 |