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HRID 27016Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/27016

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrachlorophthalic anhydrideHCID 8326—
EduktN,N-diethyl-m-toluidineHCID 66679—
EduktAluminum(III) ChlorideHCID 6451240—
Lösungsmittel1,2-DichlorobenzeneHCID 7239—
Produkt2,3,4,5-Tetrachloro-6-[4-(diethylamino)-2-methylbenzoyl]benzoic acidHCID 10433677,3%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04220357
Quelldatensatzuspto-grants-1980_09
ORD IDord-bc1b787f42e34035a981fe1e10eb945e
Quellennotizuspto-grants-1980_09