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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCesium carbonateHCID 10796—
Reactant2,2,2-TrifluoroethanethiolHCID 4133924—
Reactant2-Fluoro-5-methanesulfonyl-benzoic acidHCID 22467566—
SolventDimethylformamideHCID 6228—
Product5-Methanesulfonyl-2-(2,2,2-trifluoro-ethylsulfanyl)-benzoic acidHCID 2110031399%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557114B2
Source datasetuspto-grants-2009_07
ORD IDord-7ee2f41ac992435ea69b0e939e3ad1ca
Source noteuspto-grants-2009_07