HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Isotripiperidein
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| Reactant | 2-Methoxy-1-formylpiperidine | HCID 2723667 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Isotripiperidein | HCID 558090 | — |
Reaction Steps
28.6 g (0.2 mol) of 1-formyl-2-methoxypiperidine and 0.3 mol of methanolic HCl were refluxed for 4 hours. At atmospheric pressure in a boiling range of from 30° to 50° C. a mixture of formic acid methyl ester and methanol, which could be re-used for the preparation of 1-formyl-piperidine, was distilled off. The distillation residue was added dropwise to a solution of 21.7 g of KOH (85% strength, 0.33 mol) in methanol and the whole was refluxed for 4 hours. Working up as described in Example 4 yielded 13.3 g (80.1% of the theory) of isotripiperidein melting at 87°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04123434 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-f5b6c371913c42b2a5132cd35e8075a9 |
| Source note | uspto-grants-1978_10 |