HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → N-(2,6-dimethylphenyl)-N-(4-piperidinyl)benzeneacetamide hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | HCID 23339068 | HCID 23339068 | — |
| Product | N-(2,6-dimethylphenyl)-N-(4-piperidinyl)benzeneacetamide hydrobromide | HCID 23339026 | — |
Reaction Steps
A mixture of 5 parts of ethyl 4-[N-(2,6-dimethylphenyl)-N-(phenylacetyl)amino]-1-piperidinecarboxylate in 60 parts of hydrobromic acid solution 48% is warmed until the evolution of carbon dioxide is ceased. Heating is continued for 15 minutes at a temperature between 80°-120° C. The reaction mixture is evaporated. The solid residue is washed successively with methylbenzene and 2-propanone and dried, yielding 4.1 parts of N-(2,6-dimethylphenyl)-N-(4-piperidinyl)benzeneacetamide hydrobromide; mp. 251.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225606 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-bfa1abb1662d45aca75dc5b7909d291c |
| Source note | uspto-grants-1980_09 |