HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetyl chloride → Ethyl 4-[(4-chlorophenyl)(phenylacetyl)amino]piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Ethyl 4-[(4-chlorophenyl)amino]piperidine-1-carboxylate | HCID 2846949 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 4-[(4-chlorophenyl)(phenylacetyl)amino]piperidine-1-carboxylate | HCID 3017393 | — |
Reaction Steps
To a stirred solution of 58 parts of ethyl 4-[(4-chlorophenyl)amino]-1-piperidinecarboxylate in 240 parts of benzene is added dropwise a solution of 46.2 parts of benzeneacetyl chloride in 80 parts of benzene at a temperature between 40°-70° C. Upon completion, the whole is stirred and refluxed for 6h.15. The reaction mixture is cooled and filtered. The filtrate is washed successively with water, sodium hydrogen carbonate solution and water, then dried and evaporated in vacuo. The residue is crystallized from 1,1'-oxybisethane, yielding 47 parts of ethyl 4-[N-(4-chlorophenyl)-N-(phenylacetyl)amino]-1-piperidinecarboxylate; mp. 108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225606 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-d0e8775e28bf4a14b64ab3c30fe80e8a |
| Source note | uspto-grants-1980_09 |