HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28143Generated: October 30, 2026
Potassium Iodide → N-(2,6-dimethylphenyl)-1-propyl-4-piperidinamine
https://huagongshe.com/reaction/28143
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | N-(2,6-Dimethylphenyl)piperidin-4-amine | HCID 23339004 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2,6-dimethylphenyl)-1-propyl-4-piperidinamine | HCID 23339025 | — |
Reaction Steps
To a warm (about 40° C.) and stirred mixture of 5 parts of N-(2,6-dimethylphenyl)-4-piperidinamine, 5 parts of sodium carbonate, a few crystals of potassium iodide in 120 parts of benzene is added dropwise a solution of 5.1 parts of 1-iodopropane in 80 parts of benzene. After the addition is complete, stirring is continued for 40 hours at reflux temperature. The reaction mixture is cooled and 50 parts of water are added. The organic layer is separated, dried and evaporated in vacuo. The oily residue is distilled, yielding 10.2 parts of N-(2,6-dimethylphenyl)-1-propyl-4-piperidinamine; bp. 135° C. at 0.2 mm. pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04225606 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-72a05fb9d5f84632a59fda691ecf743c |
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| Source note | uspto-grants-1980_09 |
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