HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamide | HCID 162188 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide | HCID 20334078 | — |
Reaction Steps
To a stirred and warm (40° C.) mixture of 5 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide, 5 parts of sodium carbonate, a few crystals of potassium iodide and 200 parts of n.butanol is added 3.75 parts of bromocyclopentane and the whole is stirred and refluxed for 21h. 30. Then a second portion of 5 parts of bromocyclopentane is added and stirring at reflux temperature is continued for another 30 hours. The reaction mixture is cooled, filtered and the filtrate is evaporated. The oily residue solidifies on triturating in 1,1'-oxybisethane. The solid product is filtered off and crystallized from 1,1'-oxybisethane, yielding 1.1 parts of N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide; mp. 139.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04157393 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-adc4355ff09a4496a25b2aa2ce118de2 |
| Source note | uspto-grants-1979_06 |