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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953236Generated: November 3, 2026

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

https://huagongshe.com/reaction/1953236

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 aluminum 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 numberUS06114590
Source datasetuspto-grants-2000_09
ORD IDord-adffb0ee296b49bf82a0e4984c738cb7
Source noteuspto-grants-2000_09