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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488954생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/488954

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Pyromellitic dianhydrideHCID 6966—
반응물HexylbenzeneHCID 14109—
반응물DiisopropylethylamineHCID 81531—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물2,5-Bis(4-hexylbenzoyl)terephthalic acidHCID 22269453—

반응 조건

온도40 °C

반응 단계

To a mixture of 25.7 grams of aluminum chloride, 51.3 mL of 1,2-dichloroethane, and 10 grams of benzene-1,2,4,5-tetracarboxylic acid dianhydride (pyromellitic dianhydride) was added with cooling, a solution of 14.9 grams of hexylbenzene and 6.40 grams of diisopropylethylamine in 25 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 for an additional 15 minutes after the addition was complete, and it was then heated to 40° C. for one hour. The warm mixture was poured into a beaker with 200 grams of ice and 75 mL of concentrated hydrochloric acid and stirred overnight at room temperature. The aqueous phase was poured off, and the resulting oily solid was stirred with 500 mL of water, and the water was poured off. This water wash was repeated, and the resulting residue was dissolved in 250 mL of acetone and concentrated in vacuo. This residue was stirred with 55 mL of ethyl acetate, and the resulting solid was collected by filtration, washed with 100 mL of ethyl acetate, and dried to give 2,5-bis(4-hexylbenzoyl)terephthalic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06974877B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-ec8e0d986c114ad68d7f07cb58fc2f27
출처 메모uspto-grants-2005_12