HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28151Generated: October 25, 2026
Triethylamine → N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride
https://huagongshe.com/reaction/28151
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | N-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamide | HCID 162188 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride | HCID 23339041 | — |
Reaction Steps
To a stirred solution of 4 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide and 3 parts of N,N-diethylethanamine in 200 parts of benzene are added portionwise 4 parts of 1-iodopropane and the whole is stirred and refluxed for 47 hours. Then the second portion of 4 parts of 1-iodopropane is added and stirring and refluxing is continued for another 20 h.20. The reaction mixture is cooled and filtered. The filtrate is washed with water, dried and evaporated in vacuo. From the oily free base, the hydrochloride salt is prepared in the conventional manner in 1,1'-oxybisethane. The precipitated solid salt is filtered off and dried, yielding 3.5 parts of N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride; mp. 233.5° C.
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-e2192b2ec0f648c4994e1497b6c9c192 |
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| Source note | uspto-grants-1980_09 |
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