HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → 4-(4-Methylanilino)-1-(2-phenylethyl)piperidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Piperidinecarboxamide, 4-[(4-methylphenyl)amino]- | HCID 417239 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-(4-Methylanilino)-1-(2-phenylethyl)piperidine-4-carboxamide | HCID 20382191 | — |
Reaction Steps
A mixture of 33.35 parts of (2-bromoethyl)benzene, 35 parts of 4-[N-(4-methylphenyl)amino]-4-piperidinecarboxamide, 20 parts of N,N-diethylethanamine and 225 parts of N,N-dimethylacetamide is stirred for 4 hours at 70°-80° C. The reaction mixture is poured onto water and the product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The oily residue is poured onto water, whereupon the product is precipitated. It is filtered off and suspended twice in water. The product is filtered off again, washed with 2,2'-oxybispropane and dried, yielding 4-[N-(4-methylphenyl)amino]-1-(2-phenylethyl)-4-piperidinecarboxamide; mp. 163.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998834 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-2971d27e840949f085a11b8a15582bb3 |
| Source note | uspto-grants-1976_12 |