HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 5-Acetonyl-3-piperidinomethyl-1,2,4-oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Acetonyl-3-chloromethyl-1,2,4-oxadiazole | HCID 13824705 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Acetonyl-3-piperidinomethyl-1,2,4-oxadiazole | HCID 13824706 | 56.8% |
Reaction Steps
To a solution of 15.0 g of 5-acetonyl-3-chloromethyl-1,2,4-oxadiazole in 50 ml of THF were added dropwise 17.4 g of triethylamine and subsequently 11.0 g of piperidine. The mixture was stirred at room temperature for 24 hours and then heated under reflux for 6 hours. After cooling, the precipitated material was removed by filtration and the filtrate was evaporated in vacuo. The residue was chromatographed on silica gel using chloroform-methanol (20:1, v/v) as eluent to give 10.9 g of 5-acetonyl-3-piperidinomethyl-1,2,4-oxadiazole as a colorless solid, m.p. 66°-67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04705786 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-424a10afc27f4ca58e6791c1a2642d37 |
| Source note | uspto-grants-1987_11 |