HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → N-[1-(1H-1,2,3-benzotriazol-1-yl)propyl]-4-chlorobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Chlorobenzamide | HCID 12084 | — |
| Reactant | Propane, 1,1-diethoxy- | HCID 20858 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[1-(1H-1,2,3-benzotriazol-1-yl)propyl]-4-chlorobenzamide | HCID 18770656 | 28.5% |
Reaction Steps
A suspension of 4-chlorobenzamide (1.50 g, 9.6 mmol), propionaldehyde diethyl acetal (1.53 g, 11.6 mmol), and benzotriazole (1.15 g, 9.6 mmol) in toluene (35 mL) was treated with p-toluenesulfonic acid (100 mg, 0.53 mmol). The mixture was heated at reflux under Dean-Stark conditions for 16 hours, cooled to ambient temperature, and concentrated to dryness. The crude material was purified by flash chromatography (elution with 40% ethyl acetate/hexanes) to provide 0.860 g of the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06645968B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-5baf35a8abbc4aef94eb3a9a7b85d8fb |
| Source note | uspto-grants-2003_11 |