HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → N-(2,6-dimethylphenyl)-N-(1-ethyl-4-piperidinyl)benzeneacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-(2,6-dimethylphenyl)-N-(4-piperidinyl)benzeneacetamide | HCID 23339027 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(2,6-dimethylphenyl)-N-(1-ethyl-4-piperidinyl)benzeneacetamide | HCID 23339023 | — |
Reaction Steps
A mixture of 4 parts of iodoethane, 5 parts of N-(2,6-dimethylphenyl)-N-(4-piperidinyl)benzeneacetamide, 5 parts of sodium carbonate, a few crystals of potassium iodide in 200 parts of benzene is stirred and refluxed for 23 hours. The reaction mixture is filtered hot and the filtrate is evaporated in vacuo. The solid residue is crystallized from 1,1'-oxybisethane, yielding 2 parts of N-(2,6-dimethylphenyl)-N-(1-ethyl-4-piperidinyl)-benzeneacetamide; mp. 86.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225606 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-aab89c7a23234d3ba95280b803fe0545 |
| Source note | uspto-grants-1980_09 |