HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33693Generated: October 28, 2026
Piperidine → 1-[3-(4-Iodophenoxy)propyl]piperidine
https://huagongshe.com/reaction/33693
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(3-Chloropropoxy)-4-iodobenzene | HCID 15895520 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[3-(4-Iodophenoxy)propyl]piperidine | HCID 2304773 | — |
Reaction Steps
A suspension of 4-(3-chloro-1-propoxy)iodobenzene (5 g), piperidine (2.2 mL), sodium carbonate (2.7 g), and potassium iodide (140 mg) in n-butanol (30 mL) was heated in a 105° C. bath for 18 h. The resulting mixture was allowed to cool to room temperature, diluted with water (50 mL), and extracted with methylene chloride (2×20 mL). The combined organic phases were dried (magnesium sulfate), and evaporated in vacuo. Kugelrohr distillation of the residue (5 mm Hg, 260° C.) gave the title compound as a white crystalline solid (4.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429586B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-954f43423d5043489dc3b51ea2e8b455 |
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| Source note | uspto-grants-2008_09 |
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