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HRID 437873Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/437873

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
PatentnummerUS04032527
Quelldatensatzuspto-grants-1977_06
ORD IDord-c93422adc9154f3ab6e3c29cc6a2ae7f
Quellennotizuspto-grants-1977_06