HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873838Generated: October 26, 2026
Potassium Hydroxide → 2-(Methylsulfonyl)-4-(trifluoromethoxy)benzoic acid
https://huagongshe.com/reaction/1873838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | 2-Bromo-4-(trifluoromethoxy)benzoic acid | HCID 59447444 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(Methylsulfonyl)-4-(trifluoromethoxy)benzoic acid | HCID 59447309 | — |
Reaction Steps
To a 16 ml vial was loaded 2-bromo-4-(trifluoromethoxy)benzoic acid (225 mg, 0.79 mmol), sodium methylsulfinate (161 mg, 1.58 mmol), CuI (301 mg, 1.58 mmol), KOH (44 mg, 0.79 mmol, in 0.1 ml water) and 4 ml dimethyl sulfoxide. The reaction mixture was flushed with nitrogen, sealed and heated at 120° C. for 5 hours. After cooling to room temperature, it was diluted with 40 ml ether/ethyl acetate (1:1), 30 ml brine and 10 ml 3N HCl. The mixture was filtered through a pad of celite. The layers were separated, and the organic portion was dried over sodium sulfate, filtered and concentrated. The residue was purified with HPLC on a reverse phase column eluted with water and acetonitrile gradient solvent to give desire product as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08304434B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-e7aea2d81efd422eabbdaf4b78451d50 |
|---|
| Source note | uspto-grants-2012_11 |
|---|