HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonamide → N-tosyliminophenyliodinane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Bis(acetoxy)iodobenzene | HCID 21865429 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-tosyliminophenyliodinane | HCID 86611515 | 113.3% |
Reaction Steps
Diacetoxyiodobenzene (12.88 g, 40 mmol) was added to a solution of KOH (5.61 g, 100 mmol) and p-toluenesulfonamide (6.85 g, 40 mmol) in methanol (160 mL) at 8° C. A yellow color developed within 1 minute. The cooling bath was removed, and the solution was allowed to warm to RT with stirring for 3 hours. Water (180 mL) was added and the reaction was refrigerated overnight. The precipitate was collected by filtration and dried overnight in a vacuum dessicator to yield 10 g (66%) of a light yellow solid which was used with out further purification or characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07385066B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-35141c86b8394c1db6712fd50cc3c19e |
| Source note | uspto-grants-2008_06 |