HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417792Generated: October 31, 2026
Potassium Iodide → Ethyl 4-((4-chloro-2-nitrophenyl)amino)piperidine-1-carboxylate
https://huagongshe.com/reaction/2417792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2,5-Dichloronitrobenzene | HCID 6977 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl 4-amino-1-piperidinecarboxylate | HCID 100867 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 4-((4-chloro-2-nitrophenyl)amino)piperidine-1-carboxylate | HCID 104608 | — |
Reaction Steps
A mixture of 0.25 mole of ethyl 4-amino-1-piperidinecarboxylate, 0.3 mole of 1,4-dichloro-2-nitrobenzene, 0.3 mole of sodium carbonate, 0.2 g of potassium iodide and 160 ml of cyclohexanol was stirred at 150° C. for 40 hours. After the mixture had been cooled, toluene and water were added and the organic layer was separated off, washed three times with water, dried and evaporated. The oily residue was dissolved in hot diisopropyl ether and the solution was stirred under reflux with active charcoal, filtered and left to crystallize. Melting point: 116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04470989 |
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| Source dataset | uspto-grants-1984_09 |
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| ORD ID | ord-d3365c33bd754018a197ca286e125ff6 |
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| Source note | uspto-grants-1984_09 |
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