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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216339Generated: October 29, 2026

Triethylamine → 4-(Difluoroacetyl)-3-fluorophenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/216339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant2,2-Difluoro-1-(2-fluoro-4-hydroxyphenyl)ethan-1-oneHCID 86638492—
SolventDichloromethaneHCID 6344—
Product4-(Difluoroacetyl)-3-fluorophenyl trifluoromethanesulfonateHCID 87535561—

Reaction Steps

To 2,2-difluoro-1-(2-fluoro-4-hydroxyphenyl)ethanone (39.0 g, 0.2 mol) and Et3N (20.7 g, 0.2 mol) in CH2Cl2 at 0° C. was added Tf2O (58 g, 0.2 mol) dropwise while keeping the temperature at 0° C. The ice-salt bath was removed, and when the temperature rose to 25° C., a solution of saturated NaHCO3 was added. The aqueous phase was extracted with CH2Cl2 and the combined extracts were dried over MgSO4, and concentrated, and the residue was purified by column chromatography (PE/EA 10:1) to afford 4-(difluoroacetyl)-3-fluorophenyl trifluoromethanesulfonate as an brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193228B2
Source datasetuspto-grants-2012_06
ORD IDord-a2147d2d735341b29b214571b9408de3
Source noteuspto-grants-2012_06