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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | 2-Chloro-5-(methylsulphonyl)benzoic acid | HCID 2329132 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-Methanesulfonyl-2-(2,2,2-trifluoro-ethoxy)-benzoic acid | HCID 21100312 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07485637B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-f32491a37e2b406b8b410929d83412e2 |
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| Source note | uspto-grants-2009_02 |
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