HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonamide, 4-(hydroxymethyl)-N-methyl- → 4-Formyl-N-methylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonamide, 4-(hydroxymethyl)-N-methyl- | HCID 17981768 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Formyl-N-methylbenzenesulfonamide | HCID 14327177 | 40.8% |
Reaction Steps
A solution of 4-hydroxymethyl-N-methyl-benzenesulfonamide (1.61 g, 8.0 mmol) in DCM (50 mL) is added to a mixture of MnO2 (16.1 g, 167 mmol) in DCM (65 mL). The mixture is stirred at rt for 15 min, filtered over celite and the solvent of the filtrate is evaporated to give 4-formyl-N-methyl-benzenesulfonamide (651 mg) as a white solid; LC-MS: tR=0.68 min; 1H NMR (D6-DMSO): δ 10.08 (s, 1H), 8.12-8.07 (m, 2H), 7.98-7.94 (m, 2H), 7.68 (s br, 1H), 2.42 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039644B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-408f2e47c43e4d1c9daab3045811d9f5 |
| Source note | uspto-grants-2011_10 |