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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659982Generated: October 25, 2026

1,2,4,5-Tetrachlorobenzene → 2,3,4-Trichlorophenol

https://huagongshe.com/reaction/1659982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,4,5-TetrachlorobenzeneHCID 7270—
ReactantBenzene, (trichloromethoxy)-HCID 40773—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventO-XyleneHCID 7237—
Product2,3,4-TrichlorophenolHCID 2758297%

Reaction Steps

A mixture of trichloroanisole (0.1 g mol; 21.15 g) and 1,2,4,5-tetrachlorobenzene (10 g) in xylene (80 ml) was heated at 80° C. with aluminium trichloride (0.05 mole; 6.65 g) for five hours. Trichlorophenol was isolated in 97% yield (based on trichloroanisole) as described in Example I below. Unchanged tetrachlorobenzene, together with xylene self condensation product (total 13.25 g) was isolated from the neutral product fraction after solvent removal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04306098
Source datasetuspto-grants-1981_12
ORD IDord-c9c1696fd2094c909c2e138e64c092ea
Source noteuspto-grants-1981_12