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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723640Generated: November 3, 2026

2,2,2-Trifluoroethanol → 5-Methanesulfonyl-2-(2,2,2-trifluoro-ethoxy)-benzoic acid

https://huagongshe.com/reaction/1723640

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
Reactant2-Chloro-5-(methylsulphonyl)benzoic acidHCID 2329132—
SolventTriethylamineHCID 8471—
Product5-Methanesulfonyl-2-(2,2,2-trifluoro-ethoxy)-benzoic acidHCID 21100312—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2.13 mmol 2-chloro-5-methanesulfonyl-benzoic acid, 0.64 mmol Cu(I)Br in 5 ml NEt3 and 25 ml 2,2,2-trifluoro-ethanol was heated to 120° C. for 16 h in a sealed tube. The volatiles were removed under vacuum and the residue was taken up in 70 ml 1N HCl. Extraction with ethyl acetate drying of the combined organic fractions and evaporation yielded a residue which was purified by reversed phase preparative HPLC eluting with an acetonitrile/water gradient. Evaporation of the product fractions yielded the title compound. MS (m/e): 297.0 (M−H, 100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485637B2
Source datasetuspto-grants-2009_02
ORD IDord-f32491a37e2b406b8b410929d83412e2
Source noteuspto-grants-2009_02