HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-benzoyl-4-methyl-1,2,4-oxadiazol-5(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-benzyl-4-methyl-1,2,4-oxadiazol-5(4H)-one | HCID 21535393 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Product | 3-benzoyl-4-methyl-1,2,4-oxadiazol-5(4H)-one | HCID 89443463 | 88% |
Reaction Steps
To a solution of 3-benzyl-4-methyl-1,2,4-oxadiazol-5(4H)-one (3.87 g, 20.34 mmol, 1 eq.) in acetic acid (120 ml) was added chromium(VI) oxide (6.10 g, 61.04 mmol, 3 eq.) and stirring was allowed overnight. The reaction was quenched by addition of water and extracted with Et2O (3×50 ml). The organics were combined, washed with aq. sat. NaHCO3, dried over MgSO4 and concentrated to give 3-benzoyl-4-methyl-1,2,4-oxadiazol-5(4H)-one (3.85 g, 88% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090600B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-1eb77a2151744baaa250b50fc0f79003 |
| Source note | uspto-grants-2015_07 |