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HRID 488965作成日:2026年10月25日

Hydrochloric Acid → 2,5-Bis(2,5-dimethybenzoyl)terephthalic acid

https://huagongshe.com/reaction/488965

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Pyromellitic dianhydrideHCID 6966—
反応物P-XyleneHCID 7809—
反応物DiisopropylethylamineHCID 81531—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒1,2-DichloroethaneHCID 11—
生成物2,5-Bis(2,5-dimethybenzoyl)terephthalic acidHCID 22561363—

反応条件

温度15 °C

反応手順

A mixture of 144 grams of benzene-1,2,4,5-tetracarboxylic acid dianhydride (pyromellitic dianhydride), 439 grams of aluminum chloride, and 915 grams of 1,2-dichloroethane was cooled to 15° C. To this was added a mixture of 140 grams of p-xylene, 109 grams of N,N-diisopropylethylamine, and 426 mL of 1,2-dichloroethane over a period of 3.5 hours keeping the temperature between 15° C. and 20° C. The resulting mixture was stirred overnight at room temperature, poured into 2876 grams of ice and 1078 mL concentrated hydrochloric acid and stirred for one hour. The organic layer was washed with 7 L of water. Three liters of water was poured off and the mixture allowed to stand for 4 days, after which the remaining 3 L of water was poured off. To the resulting residue was added 7 L of ethyl acetate and 3 L of tetrahydrofuran. The organic phase was separated and concentrated in vacuo. To 92 grams of the residue was added 1910 mL of ethyl acetate and the mixture was heated to 77° C. for one hour. The mixture was cooled to room temperature and the solid was collected by filtration and dried to give 2,5-bis(2,5-dimethybenzoyl)terephthalic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06974877B2
出典データセットuspto-grants-2005_12
ORD IDord-1aa852da6f814d4ba199a95f4a4a6096
出典メモuspto-grants-2005_12