HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,4-Diphenylpiperidine → HCID 9909348, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,4-Diphenylpiperidine | HCID 2823239 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-benzyl-1H-pyrazole-3-carbaldehyde | HCID 11401199 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 9909348 | HCID 9909348 | — |
Reaction Steps
The product from step (a) (0.17 g) was dissolved in ethanol (3 ml) and a solution of 4,4-diphenylpiperidine (0.118 g) in ethanol (1 ml) added. A solution of sodium cyanoborohydride (1.0 M in tetrahydrofuran, 3.0 ml) was added and the solution stirred at room temperature for 16 hours. Silica gel was added, the solvent removed by evaporation and the crude material purified by chromatography (dichloromethane:methanol, 100:0 to 95:5) to give the product as an oil. Further purification by supercritical fluid chromatography gave the product as a solid (0.010 g), m.p. 167-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06566376B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-6483d77b263248aa82bdfde61fb0eab7 |
| Source note | uspto-grants-2003_05 |