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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701109Generated: October 26, 2026

4-Chlorobenzotrichloride → 2,4,5-Trichlorobenzotrichloride

https://huagongshe.com/reaction/1701109

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzotrichlorideHCID 21277—
ReactantSulfuryl chlorideHCID 24648—
ReactantSulfur monochlorideHCID 24807—
Reactant3,4-DichlorophenyltrichloromethaneHCID 25608—
ReactantAluminum(III) ChlorideHCID 6451240—
Product2,4,5-TrichlorobenzotrichlorideHCID 1478657447%

Reaction Steps

A solution of 4.6 g (34 mmol) of aluminum chloride and 4.6 g (34 mmol) of disulphur dichloride in 344 g (2.55 mol) of sulphuryl chloride was added dropwise to a mixture of 57.5 g (250 mmol) of p-chlorobenzotrichloride and 115 g (850 mmol) of sulphuryl chloride at 40° C. The reaction mixture was further processed in the manner described in Example 5, that is to say that, after the working up, unreacted p-chlorobenzotrichloride and 3,4-dichlorobenzotrichloride were separated off by distillation and fed to renewed chlorination with sulphuryl chloride under the conditions given here. By distillation of the combined sump fractions, 2,4,5-trichlorobenzotrichloride was obtained in a yield of 47% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04191711
Source datasetuspto-grants-1980_03
ORD IDord-52cf572afbf74898ac1c65e3b0945300
Source noteuspto-grants-1980_03