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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255798Generated: November 2, 2026

Hydrochloric Acid → Benzene, 1-chloro-4,5-difluoro-2-(trichloromethyl)-

https://huagongshe.com/reaction/2255798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCarbon TetrachlorideHCID 5943—
Reactant4-Chloro-1,2-difluorobenzeneHCID 136519—
ReactantAluminum(III) ChlorideHCID 6451240—
ProductBenzene, 1-chloro-4,5-difluoro-2-(trichloromethyl)-HCID 1096743065.4%

Reaction Steps

Into a 200 ml four-necked flask equipped with a stirrer, a reflux condenser, a thermometer and a dropping funnel, 97 ml (1 mol) of carbon tetrachloride and 26.7 g (0.2 mol) of aluminum chloride were charged, and 14.9 g (0.1 mol) of 1-chloro-3,4-difluorobenzene was gradually dropwise added over a period of 1.5 hours under reflux so that hydrochloride gas was slowly generated. The generated hydrochloride gas was absorbed by an aqueous sodium hydroxide solution. After completion of the dropwise addition, the mixture was reacted for 10 minutes. After cooling to room temperature, the reaction mixture was poured into 300 ml of ice water. The organic layer was separated and washed with 100 ml of water, then with 100 ml of 5% of sodium hydrogen carbonate aqueous solution and further with 100 ml of water. After distilling off carbon tetrachloride, the residue was distilled under reduced pressure to obtain 17.4 g (yield: 65.4%) of 2-chloro-4,5-difluorobenzotrichloride. Boiling point: 104°-106° C./8 mmHg, nD20 1.540; purity: 98.2%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05241111
Source datasetuspto-grants-1993_08
ORD IDord-16082e8045c84423829df8eadd22a4eb
Source noteuspto-grants-1993_08