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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258940Generated: October 25, 2026

1,2,3-Trichlorobenzene → 1,2,3-Trichlorobenzene

https://huagongshe.com/reaction/258940

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3-TrichlorobenzeneHCID 6895—
ReactantFuming sulfuric acidHCID 24681—
ReactantTertiary butylbenzoylbenzoic acidHCID 86734930—
SolventWaterHCID 962—
Product1,2,3-TrichlorobenzeneHCID 6895—
Product1-tert-Butylanthracene-9,10-dioneHCID 14274944—

Reaction Conditions

Temperature90 °C

Reaction Steps

To 400 parts of 10.5% oleum there was added a solution of 100 parts of tertiary butylbenzoylbenzoic acid in 600 parts of commercial trichlorobenzene. The solution was added gradually over a 30 minute period to the well-stirred oleum held at 80° to 90° C. After the addition was complete, the reaction mixture was stirred at 90° C for 4 hours, then poured into 2000 parts of cold water. The aqueous and organic layers were allowed to separate, and the aqueous layer was removed by decantation. After washing the organic layer twice with 800 part portions of water, the residual acidity was neutralized by stirring the organic layer with another 800 parts of water, sufficient 30% aqueous sodium hydroxide solution being added to achieve a pH above 7.0. A final 800 part water wash was applied, and the product was fractionally distilled. From 562 parts of crude product there was obtained 480 parts of trichlorobenzene, 80 parts of tertiary butylanthraquinone-containing product and 6 parts of residual high-boiling tar. The product was 98.4 % tertiary butylanthraquinone. The yield was 86% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035396
Source datasetuspto-grants-1977_07
ORD IDord-8a6ee73fad0f44f4b929b2314940ac52
Source noteuspto-grants-1977_07