HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-Methanesulfonyl-2-trifluoromethoxy-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzoic acid, 5-sulfino-2-(trifluoromethoxy)- | HCID 69037717 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Methanesulfonyl-2-trifluoromethoxy-benzoic acid | HCID 69039047 | — |
Reaction Steps
To 5-Sulfino-2-trifluoromethoxy-benzoic acid (0.82 g) in DMF (5 mL) was added 1.3 g of potassium carbonate, and the reaction mixture was stirred for 5 minutes before methyl iodide (0.66 mL) was added. The reaction mixture was then stirred at room temperature for 60 hours. After such time the reaction mixture was concentrated in vacuo, and the residue was treated with 1N NaOH (10 mL) and THF (4 mL). The reaction mixture was stirred for a further 2 hours at room temperature. After such time the solution was acidified with concentrated HCl solution. THF was then removed in vacuo) and the precipitate was isolated by filtration and washed several times with water to yield the title compound. MS (m/e): 283.0 (M−H, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07319099B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-2198b4e6d33d45cf9a4817f95f586439 |
| Source note | uspto-grants-2008_01 |