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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80312Generated: October 25, 2026

Piperidine → 1-[Tris(4-methoxyphenyl)methyl]piperidine

https://huagongshe.com/reaction/80312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4,4',4''-Trimethoxytrityl chlorideHCID 630505—
SolventAcetonitrileHCID 6342—
SolventHexaneHCID 8058—
Product1-[Tris(4-methoxyphenyl)methyl]piperidineHCID 6742765649%

Reaction Steps

4,4′,4″-trimethoxytrityl chloride (0.51 g, 1.38 mmol) (Aldrich) was dissolved in acetonitrile (8 mL) (Wako Pure Chemical Industries, Ltd.), and piperidine (0.70 g, 8.22 mmol) (Wako Pure Chemical Industries, Ltd.) was added thereto. The mixture was refluxed for 1 hour, and then the solvent was distilled off under reduced pressure. A saturated aqueous solution of sodium hydrogen carbonate (Wako Pure Chemical Industries, Ltd.) was added to the concentrated residue, and mixture was extracted with ethyl acetate (Wako Pure Chemical Industries, Ltd.). The organic layer was washed with water and brine. After that, the organic layer was dried with anhydrous sodium sulfate (Wako Pure Chemical Industries, Ltd.), and the solvent was distilled off under reduced pressure. The residue was subjected to alumina column chromatography (chloroform (Wako Pure Chemical Industries, Ltd.):n-hexane (Wako Pure Chemical Industries, Ltd.)=1:4 as an eluent), to thereby obtain the title compound (0.28 g, 49% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846012B2
Source datasetuspto-grants-2014_09
ORD IDord-85dda6bb728945c5a54a50350128dcb1
Source noteuspto-grants-2014_09