HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 5-Chloro-2-(methylsulfonyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 5-Chloro-2-(methylthio)benzonitrile | HCID 59845693 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Chloro-2-(methylsulfonyl)benzonitrile | HCID 66970048 | — |
Reaction Steps
(Step 2) To a solution of 5-chloro-2-(methylsulfanyl)benzonitrile obtained in Step 1 (1.0 g) in acetonitrile (15 ml) was added dropwise a solution of Oxone® (6.98 g) in water (20 ml). The resulting mixture was stirred at room temperature for 5 hr. Oxone® (1.2 g) was added, and the mixture was stirred overnight at room temperature. To the reaction mixture was added water (25 ml), and the resulting mixture was stirred at 0° C. for 3 hr. The precipitate was collected by filtration, washed with water, and dried to give 5-chloro-2-(methylsulfonyl)benzonitrile (0.92 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07985863B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-9edd5c5efe7247bc956ddd4c5a26b48e |
| Source note | uspto-grants-2011_07 |