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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488959생성일: 2026년 10월 25일

Hydrochloric Acid → 2,5-Bis(4-dodecylbenzoyl)terephthalic acid

https://huagongshe.com/reaction/488959

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Pyromellitic dianhydrideHCID 6966—
반응물DodecylbenzeneHCID 31237—
반응물DiisopropylethylamineHCID 81531—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2,5-Bis(4-dodecylbenzoyl)terephthalic acidHCID 22269479—

반응 조건

온도16 °C

반응 단계

To a mixture of 492 grams of aluminum chloride and 988 mL of 1,2-dichloroethane was added 192 grams of benzene-1,2,4,5-tetracarboxylic acid dianhydride (pyromellitic dianhydride). The resulting mixture was cooled to 16° C. and a solution of 434 grams of 1-dodecylbenzene, 123 grams of diisopropylethylamine and 480 mL of 1,2-dichloroethane was added over a period of 3.5 hours, keeping the temperature between 15° C. and 20° C. during the addition. The mixture was stirred overnight at room temperature and poured into a beaker of 1000 grams of ice and 1000 grams concentrated hydrochloric acid. The mixture was stirred for one hour and the liquid was poured from the coagulate. The mixture was divided into 800 mL portions and each portion was worked up as follows. To 800 mL of the mixture was added 800 mL of tetrahydrofuran, 800 mL of ethyl acetate and 800 mL of water. The mixture was stirred and phase split. The organic phase was filtered and the filtrate was concentrated in vacuo. The resulting residues were combined. To 127 grams of the combined residue was added 800 mL of ethyl acetate and the resulting mixture was stirred until a suspension of a fine solid resulted. The solid was collected by filtration and washed with 50 mL of ethyl acetate. The solid was dried to give 2,5-bis(4-dodecylbenzoyl)terephthalic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06974877B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-1efb02decaaa4d129934a9f433d98494
출처 메모uspto-grants-2005_12