HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 86670499, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86670499 | HCID 86670499 | — |
Reaction Steps
An equimolar mixture of 25.0 g (0.17 mol) 4-carboxybenzaldehyde and 26.7 g (0.17 mol) benzenesulfonamide was placed into toluene. 100 mg p-toluenesulfonic acid was added as a catalyst. The mixture was then heated under reflux on a water separator until the theoretically calculated quantity of water had separated. After cooling to room temperature, the precipitated solid was filtered off and dried under vacuum. Yield: 45.7 g (94.8%); 1H-NMR (400 MHz, DMSO-d6): δ [ppm]=7.59 (m, 2H); 7.78 (d, 1H); 8.02 (m, 2H); 8.12 (d, 2H); 8.18 (d, 2H); 9.30 (s, 1H); 13C-NMR (400 MHz, DMSO-d6): δ [ppm]=127.8; 129.7; 131.4; 134.1; 135.8; 136.0; 137.9; 166.5; 171.2; 192.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08323356B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-e1d4d7bf453541dc8fcc959b068e1d90 |
| Source note | uspto-grants-2012_12 |