HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 5-Chloro-2-hydroxy-N-methyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-chloro-2-methoxy-N-methylbenzenesulfonamide | HCID 2987885 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Chloro-2-hydroxy-N-methyl-benzenesulfonamide | HCID 18768102 | 64.2% |
Reaction Steps
To a solution of sodium hydride (60% in mineral oil, 90.24 mg, 2.25 mmol) in dry dimethyl formamide was added thiophenol (0.225 ml, 2.25 mmol) dropwise. To this was then added 5-Chloro-2-methoxy-N-methyl-benzenesulfonamide (531 mg, 2.25 mmol) followed by refluxing for 4 hours. The reaction mixture was cooled, diluted with ethyl acetate and washed with a 1N sulfuric acid solution. The organic layer was separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Chromatography on silica gel yielded the above titled compound (320 mg, 53% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06649611B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-8d3749d4f25943e7b04a0ddc71f49585 |
| Source note | uspto-grants-2003_11 |