HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1-(3-Phenyl-[1,2,4]oxadiazol-5-yl)-piperidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 8-(3-Phenyl-1,2,4-oxadiazol-5-yl)-1,4-dioxa-8-azaspiro[4.5]decane | HCID 20952653 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(3-Phenyl-[1,2,4]oxadiazol-5-yl)-piperidin-4-one | HCID 68290212 | — |
Reaction Steps
A mixture of 8-(3-phenyl-[1,2,4]oxadiazol-5-yl)-1,4-dioxa-8-aza-spiro[4.5]decane (660 mg), conc. aqueous HCl (5 mL) and water (5 mL) is kept at room temperature over night. The mixture is basified with conc. aqueous ammonia and the precipitate is filtered off and dissolved in dichloromethane. The resulting solution is dried over Na2SO4 and concentrated in vacuo to give the title compound. TLC: rf=0.33 (silica gel, hexane/ethyl acetate 2:1); Mass spectrum (ESI+): m/z=244 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822471B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-4bf4a52a7c9c44a6950c58f3f18ba9bf |
| Source note | uspto-grants-2014_09 |