HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26758Generated: October 30, 2026
Potassium Iodide → HCID 23339043, compound
https://huagongshe.com/reaction/26758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | 4-chloro-N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide | HCID 23338995 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 23339043 | HCID 23339043 | — |
Reaction Steps
To a stirred and refluxing mixture of 5 parts of 4-chloro-N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide, 5 parts of sodium carbonate, 0.4 parts of potassium iodide and 200 parts of butanol is added 4.7 parts of 1-iodopropane and the whole is stirred and refluxed for 22 hours. Then a second portion of 4.5 parts of 1-iodopropane is added and stirring and refluxing is continued for 27h.30. The reaction mixture is cooled, filtered and the filtrate is evaporated. The semi-solid residue is dissolved in methylbenzene. The solution is filtered from some impurities and the filtrate is evaporated again. The residue is crystallized from 1,1'-oxybisethane at -10° C.; yielding 0.9 parts of 4-chloro-N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide; mp. 118.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04151286 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-873fbda636df455a949aad67303deb6c |
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| Source note | uspto-grants-1979_04 |
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