HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604402Generated: October 29, 2026
Potassium Iodide → HCID 10879264, compound
https://huagongshe.com/reaction/604402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1,10-Dibromodecane | HCID 221483 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 10879264 | HCID 10879264 | — |
Reaction Steps
The synthesis was performed according to the procedure described in example 157 using reagents 1,10-dibromodecane (30 mmol), potassium phthalimide (15 mmol), and catalytic amounts of potassium iodide in the first step. The product (12.5 mmol), piperidine (50 mmol) and catalytic amounts of potassium iodide were refluxed in acetone for 12 hours. Solvent and piperidine were evaporated. The residue was treated with hydrochloric acid (2N), with potassium carbonate solution and then extracted with methylene chloride. The solvent was removed under reduced pressure, and the residue was refluxed in hydrochloric acid (6N) for 12 hours. The solution was neutralized with potassium carbonate solution and extracted with methylene chloride. The organic layer was evaporated, and the final product purified by flash chromatography (eluent: methylene chloride/triethylamine/methanol (90/10/2)). The solvent was removed under reduced pressure. The residue was crystallized with oxalic acid from diethyl ether/ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910605B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-bcadab41211f476f9334eaca952c71ef |
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| Source note | uspto-grants-2011_03 |
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