HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → ethyl N-(2,4,6-trimethylphenylacetyl)-piperidine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl piperidine-2-carboxylate | HCID 27517 | — |
| Reactant | 2,4,6-Trimethylbenzeneacetyl chloride | HCID 11030754 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl N-(2,4,6-trimethylphenylacetyl)-piperidine-2-carboxylate | HCID 14883010 | 95.9% |
Reaction Steps
223 g (1.125 mol) of mesityleneacetyl chloride are added dropwise at 0° to 10° C. to 182 ml (1.157 mol) of ethyl pipecolinate and 162 ml (1.157 mol) of triethylamine in 1,200 ml of absolute tetrahydrofuran (THF), followed by stirring for 1 hour at room temperature. After the mixture has been stirred into 5 liters of ice water and 500 ml of 1 N HCl, the product is filtered off with suction, washed with water and dried in vacuo at 50° C. over P2O5. 342.3 g (95.2% of theory) of ethyl N-(2,4,6-trimethylphenylacetyl)-piperidine-2-carboxylate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985063 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-193ecb6fe6c54afdaf079156e523890e |
| Source note | uspto-grants-1991_01 |