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HRID 2931作成日:2026年10月24日

4-Chloro-o-xylene → 2,2'-Dichloro-4,4',5,5'-tetramethylbenzophenone

https://huagongshe.com/ja/reaction/2931

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-o-xyleneHCID 32886—
反応物Oxalyl chlorideHCID 65578—
反応物4,4'-Carbonyldiphthalic anhydrideHCID 75498—
生成物2,2'-Dichloro-4,4',5,5'-tetramethylbenzophenoneHCID 15027172—

反応手順

Specific benzophenonetetracarboxylic dianhydrides preferred in this invention are readily available from commercial sources or synthesis. For instance, 3,3',4,4'-benzophenonetetracarboxylic dianhydride (D1) is available from Aldrich Chemical Co., Inc. (1001 W. St. Paul Ave., Milwaukee, Wis. 53233). 2,2'-Dichloro-4,4',5,5'-benzophenone tetracarboxylic dianhydride (D2) is available from 4-chloro-o-xylene by Friedel-Crafts acylation with oxalyl chloride to give 2,2'dichloro-4,4',5,5',-tetramehtylbenzophenone, followed by oxidation with nitric acid and dehydration of the resulting tetracarboxylic acid as described by Falcigno, et al., J. Poly. Sci. 1992, 30, 1433.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731405
出典データセットuspto-grants-1998_03
ORD IDord-9d4147d3edea46ffb150787b3152cac8
出典メモuspto-grants-1998_03