HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic acid, p-nitro-, acetylhydrazide → 2-Methyl-5-(4-nitrophenyl)-1,3,4-oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic acid, p-nitro-, acetylhydrazide | HCID 3332418 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | 2-Methyl-5-(4-nitrophenyl)-1,3,4-oxadiazole | HCID 540416 | 89% |
Reaction Steps
A solution of 4-nitro-benzoic acid N′-acetyl-hydrazide (200 mg, 8.9 mmol) in distilled POCl3 (4 mL) was refluxed at 110° C. under nitrogen for 6 hours. The reaction mixture was concentrated and the residue was quenched with 10% NaOH solution. The resulting precipitate was collected by filtration to afford 160 mg (89%) of 2-Methyl-5-(4-nitro-phenyl)-[1,3,4]oxadiazole. 1H NMR: (CDCl3): δ 8.38 (d, 2H), 8.24 (d, 2H), 2.7 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039463B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-fa2e928ea702448db338410c903e51be |
| Source note | uspto-grants-2011_10 |