Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | HCID 12354273 | HCID 12354273 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58130401 | HCID 58130401 | 74% |
Reaction Steps
3-Methyl-1H-benzo[f]thiochromen-1-one (1.0 mmol, 176 mg), iodine (1.2 mmol, 305 mg) and ceric ammonium nitrate (1.1 mmol, 603 mg) were dissolved in acetonitrile (4.0 mL), and the solution was stirred under a nitrogen atmosphere at 60° C. for 4 hours. After the disappearance of the starting materials was confirmed by thin-layer chromatography, the reaction solution was poured into a solution of a 10% saturated aqueous sodium thiosulfate solution under ice-cooling to terminate the reaction. The organic substances were extracted with methylene chloride, the obtained organic layer was dried over magnesium sulfate, and the solvents were evaporated under reduced pressure. The residue was purified by silica gel column chromatography, and the title compound (0.74 mmol, 260 mg) was obtained in a 74% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08222429B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-2243252b6be7412eae9f7818f4da80d2 |
|---|
| Source note | uspto-grants-2012_07 |
|---|