HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 1,2-Bis(2-(trifluoromethyl)phenyl)disulfane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-(Trifluoromethyl)benzenethiol | HCID 2777889 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,2-Bis(2-(trifluoromethyl)phenyl)disulfane | HCID 11325681 | 88.3% |
Reaction Steps
A solution of 2-(trifluoromethyl)benzenethiol (0.185 mL, 1.40 mmol) in wet acetonitrile (1:5 water/acetonitrile) was added Iodine (0.178 g, 0.702 mmol) and allowed to stir over night at room temperature. The reaction was concentrated, then diluted with EtOAc and quenched with aqueous sodium thiosulfate, extracted and dried organic with brine, Na2SO4, filtered and concentrated to afford the title compound (219 mg, 44% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022223B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-538faa91f2724abd801a42579087118f |
| Source note | uspto-grants-2011_09 |