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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27016Generated: October 26, 2026

Tetrachlorophthalic anhydride → 2,3,4,5-Tetrachloro-6-[4-(diethylamino)-2-methylbenzoyl]benzoic acid

https://huagongshe.com/reaction/27016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrachlorophthalic anhydrideHCID 8326—
ReactantN,N-diethyl-m-toluidineHCID 66679—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichlorobenzeneHCID 7239—
Product2,3,4,5-Tetrachloro-6-[4-(diethylamino)-2-methylbenzoyl]benzoic acidHCID 10433677.3%

Reaction Steps

A mixture of tetrachlorophthalic anhydride (21.4 g.), N,N-diethyl-m-toluidine (41 g.), aluminum chloride (30 g.) and o-dichlorobenzene (90 ml.) was heated (75°-95° C.) during one to two hours, then diluted with ice-water. The o-dichlorobenzene layer was separated and steam distilled. The residue was heated with dilute sulfuric acid. The mixture was poured onto ice and made alkaline. The resulting oil was heated in concentrated sulfuric acid. Dilution with water and purification of the product with toluene and hexane afforded 2-(2-methyl-4-(diethylamino)benzoyl)-3,4,5,6-tetrachlorobenzoic acid (IV: Y2 =CH3, Y'4 =(CH3CH2)2N, Z4 =Z"5 =Z"6 =Z7 =Cl) (26 g., m.p. 117° C. with sublimation).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220357
Source datasetuspto-grants-1980_09
ORD IDord-bc1b787f42e34035a981fe1e10eb945e
Source noteuspto-grants-1980_09