HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivalaldehyde → N-(1-(1H-1,2,3-benzotriazol-1-yl)-2,2-dimethylpropyl)-4-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | 4-Methylbenzamide | HCID 69274 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(1-(1H-1,2,3-benzotriazol-1-yl)-2,2-dimethylpropyl)-4-methylbenzamide | HCID 11450124 | 68.1% |
Reaction Steps
A suspension of p-toluamide (4.11 g, 30.4 mmol), pivaldehyde (2.62 g, 30.4 mmol), and benzotriazole (3.62 g, 30.4 mmol) in toluene (200 mL) was treated with p-toluenesulfonic acid (286 mg, 1.52 mmol). The solution was heated at reflux under Dean-Stark conditions for 10 hours, cooled gradually to ambient temperature, and further cooled to 5° C. The white precipitate which formed was collected by filtration and was washed with 50% diethyl ether/hexanes (100 mL) to provide 6.67 g of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06495576B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-fcab0424c38c4528ba14b1703badd321 |
| Source note | uspto-grants-2002_12 |