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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4,4',4''-Trimethoxytrityl chloride | HCID 630505 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-[Tris(4-methoxyphenyl)methyl]piperidine | HCID 67427656 | 49% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846012B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-85dda6bb728945c5a54a50350128dcb1 |
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| Source note | uspto-grants-2014_09 |
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