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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449836Generated: November 2, 2026

1,2,3,4-Tetrafluoro-5-(trifluoromethyl)benzene → 1,2,3,4-Tetrafluoro-5-(trichloromethyl)benzene

https://huagongshe.com/reaction/1449836

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-Tetrafluoro-5-(trifluoromethyl)benzeneHCID 2733690—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1,2,3,4-Tetrafluoro-5-(trichloromethyl)benzeneHCID 15346007—

Reaction Steps

85 g (0.64 mol) of aluminium chloride (anhydrous) are initially introduced into 500 ml of methylene chloride, and 109 g (0.5 mol) of 2,3,4,5-tetrafluoro-benzotrifluoride are added dropwise at room temperature, while stirring. The mixture is then subsequently stirred at 40° C. for 1 hour, allowed to cool and poured onto 600 g of ice, the organic phase is separated off, the aqueous phase is extracted with ether and the combined phases are washed with water and dried over anhydrous magnesium sulphate. After concentration, the residue is distilled. 108.3 g (81% of theory) of product are obtained; boiling point: 89°-90° C./22 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599980
Source datasetuspto-grants-1997_02
ORD IDord-1e894b0ea5a94d878a113683cce3a45f
Source noteuspto-grants-1997_02