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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413284Generated: October 28, 2026

4,4-Diphenylpiperidine → HCID 9909348, compound

https://huagongshe.com/reaction/413284

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4-DiphenylpiperidineHCID 2823239—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-benzyl-1H-pyrazole-3-carbaldehydeHCID 11401199—
SolventEthanolHCID 702—
ProductHCID 9909348HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566376B1
Source datasetuspto-grants-2003_05
ORD IDord-6483d77b263248aa82bdfde61fb0eab7
Source noteuspto-grants-2003_05