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HRID 258940作成日:2026年10月26日

1,2,3-Trichlorobenzene → 1,2,3-Trichlorobenzene

https://huagongshe.com/reaction/258940

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3-TrichlorobenzeneHCID 6895—
反応物Fuming sulfuric acidHCID 24681—
反応物Tertiary butylbenzoylbenzoic acidHCID 86734930—
溶媒WaterHCID 962—
生成物1,2,3-TrichlorobenzeneHCID 6895—
生成物1-tert-Butylanthracene-9,10-dioneHCID 14274944—

反応条件

温度90 °C

反応手順

To 400 parts of 10.5% oleum there was added a solution of 100 parts of tertiary butylbenzoylbenzoic acid in 600 parts of commercial trichlorobenzene. The solution was added gradually over a 30 minute period to the well-stirred oleum held at 80° to 90° C. After the addition was complete, the reaction mixture was stirred at 90° C for 4 hours, then poured into 2000 parts of cold water. The aqueous and organic layers were allowed to separate, and the aqueous layer was removed by decantation. After washing the organic layer twice with 800 part portions of water, the residual acidity was neutralized by stirring the organic layer with another 800 parts of water, sufficient 30% aqueous sodium hydroxide solution being added to achieve a pH above 7.0. A final 800 part water wash was applied, and the product was fractionally distilled. From 562 parts of crude product there was obtained 480 parts of trichlorobenzene, 80 parts of tertiary butylanthraquinone-containing product and 6 parts of residual high-boiling tar. The product was 98.4 % tertiary butylanthraquinone. The yield was 86% of theory.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04035396
出典データセットuspto-grants-1977_07
ORD IDord-8a6ee73fad0f44f4b929b2314940ac52
出典メモuspto-grants-1977_07