HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866053Generated: October 30, 2026
Water → 4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidine
https://huagongshe.com/reaction/866053
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Piperidinecarboxamide | HCID 3772 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 1-(Chloromethyl)-4-propoxybenzene | HCID 12249108 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidine | HCID 19040932 | 79.1% |
Reaction Steps
The method taught by R. A. Farr et al, J. Org. Chem. 1981, 46, 1212-1215, was used in the following two-step preparation. A vigorously stirred solution of 16.5 grams (0.129 mole) of 4-aminocarbonylpiperidine, 25.0 grams (0.135 mole) of 4-propoxyphenylmethyl chloride, and 19.4 grams (0.193 mole) of potassium bicarbonate in 200 mL of toluene was heated at reflux for 6.5 hours. The reaction mixture was then cooled, water was added, and the mixture was extracted with ethyl acetate. The extract was washed with two portions of an aqueous solution saturated with sodium chloride. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a solid residue, which was slurried in pentane and collected by filtration, yielding 28.2 grams of 4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidine, mp 142°-146° C. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05569664 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-0bdf3c4da8a24475917f7120ee4b3488 |
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| Source note | uspto-grants-1996_10 |
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