HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → N-(2-fluoro-3-formyl-phenyl)-4-trifluoromethyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(2-fluoro-3-hydroxymethyl-phenyl)-4-trifluoromethyl-benzenesulfonamide | HCID 57963251 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-fluoro-3-formyl-phenyl)-4-trifluoromethyl-benzenesulfonamide | HCID 57963257 | 96% |
Reaction Steps
To N-(2-fluoro-3-hydroxymethyl-phenyl)-4-trifluoromethyl-benzenesulfonamide (33, 634 mg, 1.82 mmol) in 7 mL of tetrahydrofuran, Dess-Martin periodane (847 mg, 2.00 mmol) and sodium bicarbonate (2 g) were added. The reaction was stirred at room temperature for one hour, then poured into saturated aqueous sodium thiosulfate solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under vacuum and the residue was purified by silica gel column chromatography eluting with 15% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound (34, 607 mg, 96%). MS(ESI) [M−H+]−=346.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153641B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-877d82c9f2ba4adb8f1e62a25faeb942 |
| Source note | uspto-grants-2012_04 |