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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530976Generated: October 30, 2026

Trifluoromethanesulfonic anhydride → Ethyl 2-ethoxy-4'-fluoro-6-(((trifluoromethyl)sulfonyl)oxy)biphenyl-4-carboxylate

https://huagongshe.com/reaction/530976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantEthyl 2-ethoxy-4'-fluoro-6-hydroxybiphenyl-4-carboxylateHCID 90423930—
SolventPyridineHCID 1049—
ProductEthyl 2-ethoxy-4'-fluoro-6-(((trifluoromethyl)sulfonyl)oxy)biphenyl-4-carboxylateHCID 117992433—

Reaction Steps

Trifluoromethanesulfonic anhydride (8.66 mL) was added at 0° C. to a mixture of ethyl 2-ethoxy-4′-fluoro-6-hydroxybiphenyl-4-carboxylate (13.0 g) and pyridine (80 mL), and the resultant mixture was stirred at the same temperature as above for 20 minutes. The reaction mixture was passed through a short silica gel (NH) column, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (15.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353108B2
Source datasetuspto-grants-2016_05
ORD IDord-4b69b4ce59544614ade2e82a8299df26
Source noteuspto-grants-2016_05