HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(Piperidin-4-ylideneaminooxy)-piperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Piperidone | HCID 33721 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | tert-Butyl 4-(aminooxy)piperidine-1-carboxylate | HCID 24729482 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Piperidin-4-ylideneaminooxy)-piperidine-1-carboxylic acid tert-butyl ester | HCID 58333598 | 99.2% |
Reaction Steps
To a solution of 4-piperidinone (2.5 mmol) in 25 mL of DCM, was added 69b (0.43 g, 2 mmol). The mixture was stirred at room temperature for 2 h. NaOAc (0.27 g, 2 mmol) and ethanol (10 mL) were added and the reaction mixture was heated at 70° C. for 2 h. The solution was allowed to cool down to room temperature and the ethanol was evaporated. The residue was extracted with ethyl acetate, washed with water, dried and concentrated to give 0.59 g of 69c.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08293729B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-18f80c420105424ab0f2180faf278b0b |
| Source note | uspto-grants-2012_10 |