HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225699Generated: October 29, 2026
Hydrochloric Acid → 5-Methanesulfonyl-2-(2,2,2-trifluoro-ethylsulfanyl)-benzoic acid
https://huagongshe.com/reaction/225699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,2,2-Trifluoroethanethiol | HCID 4133924 | — |
| Reactant | 2-Fluoro-5-methanesulfonyl-benzoic acid | HCID 22467566 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Methanesulfonyl-2-(2,2,2-trifluoro-ethylsulfanyl)-benzoic acid | HCID 21100313 | 99% |
Reaction Steps
To a solution of 4.58 mmol 2-fluoro-5-methanesulfonyl-benzoic acid (Example B4(b)) in 6 ml N,N-dimethylformamide were added 13.8 mol cesium carbonate and 9.16 mmol 2,2,2-trifluoro-ethanethiol and the mixture was stirred at 90° C. for 30 min. The reaction mixture was then cooled to room temperature and acidified to pH1 by addition of hydrochloric acid before being extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulfate and concentrated in vacuo to afford the title compound as a red-brown solid which was used in the next step without further purification (yield 99%). MS (m/e): 312.9 ([M−H]−, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07557114B2 |
|---|
| Source dataset | uspto-grants-2009_07 |
|---|
| ORD ID | ord-7ee2f41ac992435ea69b0e939e3ad1ca |
|---|
| Source note | uspto-grants-2009_07 |
|---|