HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,2,4-Trifluoro-5-(methylsulfonyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,5-Trifluorobenzenesulfinic acid | HCID 57241375 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,2,4-Trifluoro-5-(methylsulfonyl)benzene | HCID 46739396 | 98% |
Reaction Steps
To 2,4,5-trifluoro-benzenesulfinic acid (2.0 g) in DMF (17 mL) was added 4.3 g of potassium carbonate, and the reaction mixture was stirred for 5 minutes before methyl iodide (2.2 mL) was added. The reaction mixture was then stirred at room temperature for 60 hours. After such time, water (30 mL) was poured onto the reaction mixture, and the reaction mixture was extracted with diethylether several times. The combined organic phases were dried with sodium sulfate, and the remaining mixture was distilled to yield the title compound as a light yellow oil (2.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07319099B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-03f9d66dc591461693751a7b38da6516 |
| Source note | uspto-grants-2008_01 |