HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 4-(1,3,4-Oxadiazol-2-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 22631214 | HCID 22631214 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 4-(1,3,4-Oxadiazol-2-yl)benzaldehyde | HCID 22630863 | 72% |
Reaction Steps
To the product from step B (175 mg, 0.80 mmol) in a 1:1 mixture of tetrahydrofuran/water (2 mL) at room temperature was added p-toluenesulfonic acid (50 mg, 0.3 mmol). The reaction mixture was stirred at room temperature for 1 h, and partitioned between dichloromethane and sat. aq. NaHCO3. The organic layer was dried with Na2SO4, and concentrated in vacuo to give 100 mg (72%) of the title product, which was used without further purification. MS 175 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825170B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-f806d48a5f7f4ab3aaffcf3af5ca9584 |
| Source note | uspto-grants-2004_11 |