HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3543-21-3
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Reactant | HCID 67366133 | HCID 67366133 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3543-21-3 | HCID 59401689 | 151.7% |
Reaction Steps
11 g KOH were added to a solution of 7.3 g (1 eq) benzyloxycarbonyl-4-phenyl-4-(pyrrolidin-1-yl)piperidine in 100 ml ethanol and the reaction mixture was refluxed for 24 h. The reaction course was monitored by thin-layer chromatography (20% MeOH/CHCl3). Once the conversion was complete, the solvent was distilled off completely and the residue mixed with 100 ml water and extracted 3 times with 100 ml CHCl3. The combined organic phases were dried with Na2SO4. Following removal of the solvent under reduced pressure, 7 g of crude product were obtained in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206156B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-011bf44ee23a48e284d50fa83b8efb66 |
| Source note | uspto-grants-2015_12 |