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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261148Generated: October 25, 2026

Water → 4-Chloro-2-fluoro-1-(2,2,2-trifluoroethoxy)benzene

https://huagongshe.com/reaction/1261148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,1,1-Trifluoro-2-iodoethaneHCID 67709—
Reactant4-Chloro-2-fluorophenolHCID 181975—
ReactantPotassium FluorideHCID 522689—
SolventMethanolHCID 887—
Product4-Chloro-2-fluoro-1-(2,2,2-trifluoroethoxy)benzeneHCID 59506748—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 4-Chloro-2-fluoro-phenol (521, 5.0 g, 0.034 mol) in methanol (50.0 mL) was added potassium fluoride (2.2 g, 0.038 mol). The solvent was removed. The resulting salt was added to N,N-dimethylformaldehyde (25 mL), followed by adding 1,1,1-trifluoro-2-iodo-ethane (8.60 g, 40.9 mmol). The reaction was stirred at 50° C. overnight. The reaction was poured into water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 20% ethyl acetate in hexane to give colorless oil (522, 2.0 g, 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470818B2
Source datasetuspto-grants-2013_06
ORD IDord-9f8d47da56a4470ea1624567d4c59c22
Source noteuspto-grants-2013_06