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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531010Generated: October 30, 2026

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

https://huagongshe.com/reaction/531010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantEthyl 4'-fluoro-2-hydroxy-6-propoxybiphenyl-4-carboxylateHCID 90424026—
SolventPyridineHCID 1049—
ProductEthyl 4'-fluoro-2-propoxy-6-(((trifluoromethyl)sulfonyl)oxy)biphenyl-4-carboxylateHCID 117992413—

Reaction Steps

Trifluoromethanesulfonic anhydride (20.1 mL) was added at 0° C. to a mixture of ethyl 4′-fluoro-2-hydroxy-6-propoxybiphenyl-4-carboxylate (31.5 g) and pyridine (200 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 (44.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353108B2
Source datasetuspto-grants-2016_05
ORD IDord-e93a7877ec3e4128961b5947be96ccde
Source noteuspto-grants-2016_05