HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 1-[1-(4-Nitrophenyl)piperidin-4-yl]-4-(oxetan-3-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Reactant | 1-[1-(4-Nitrophenyl)piperidin-4-yl]piperazine monohydrochloride | HCID 117666964 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[1-(4-Nitrophenyl)piperidin-4-yl]-4-(oxetan-3-yl)piperazine | HCID 117667063 | 63.2% |
Reaction Steps
A mixture of 1-[1-(4-nitrophenyl)piperidin-4-yl]piperazine monohydrochloride (1 g), oxetan-3-one (300 mg), sodium triacetoxyborohydride (1.02 g), dichloromethane (20 mL), acetic acid (1 mL), and chloroform (30 mL) was stirred at room temperature for 2 days. To the reactant were added a saturated aqueous sodium hydrogen carbonate solution and chloroform, followed by liquid separation. The organic phase was washed with saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent; chloroform:methanol=1:0-9:1) to obtain 1-[1-(4-nitrophenyl)piperidin-4-yl]-4-(oxetan-3-yl)piperazine (670 mg) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09085540B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-a8800b6858194b22ae0b926a14ade9cb |
| Source note | uspto-grants-2015_07 |