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HRID 437873作成日:2026年10月25日

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

https://huagongshe.com/reaction/437873

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrachlorophthalic anhydrideHCID 8326—
反応物N,N-diethyl-m-toluidineHCID 66679—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物2,3,4,5-Tetrachloro-6-[4-(diethylamino)-2-methylbenzoyl]benzoic acidHCID 10433677.3%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04032527
出典データセットuspto-grants-1977_06
ORD IDord-c93422adc9154f3ab6e3c29cc6a2ae7f
出典メモuspto-grants-1977_06