HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropyl Ether → Benzyl 4-(2-oxoethyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Phenylmethyl 4-(2-chloro-2-oxoethyl)-1-piperidinecarboxylate | HCID 20479781 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Benzyl 4-(2-oxoethyl)piperidine-1-carboxylate | HCID 22278282 | 95.7% |
Reaction Steps
A mixture of 90 parts of (phenylmethyl) 4-(2- chloro-2-oxoethyl)-1-piperidinecarboxylate, 90 parts of N,N-dimethylacetamide 6 parts of a thiophene solution and 438 parts of 2,2'-oxybispropane was hydrogenated at normal pressure and at room temperature in the presence of 5 parts of palladium-on-charcoal 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was taken up in water. The separated organic layer was dried, filtered and evaporated, yielding 75 parts (95.7%) of (phenylmethyl) 4-(2-oxoethyl)-1-piperidinecarboxylate as a residue (interm. 7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112825 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-f0109f1715e245e9a194756130010a09 |
| Source note | uspto-grants-1992_05 |