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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488975생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/488975

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Pyromellitic dianhydrideHCID 6966—
반응물DiisopropylethylamineHCID 81531—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물2-EthylhexylbenzeneHCID 22117015—
용매1,2-DichloroethaneHCID 11—
생성물2,5-Bis(4-(2-ethylhexyl)benzoyl)terephthalic acidHCID 22269444—

반응 단계

A mixture of 215.39 grams of aluminum chloride, 83.89 grams of benzene-1,2,4,5-tetracarboxylic acid dianhydride (pyromellitic dianhydride), and 533.85 grams of 1,2-dichloroethane was stirred at 15° C. to 16° C. To this mixture was added a solution of 183 grams of (2-ethylhexyl)benzene and 53.685 grams of N,N-diisopropylethylamine in 198 mL of 1,2-dichloroethane over a period of 3.5 hours keeping the reaction temperature between 15° C. and 20° C. The mixture was stirred overnight at room temperature and then added to 400 g of ice and 400 mL concentrated hydrochloric acid. This mixture was stirred for 1 hour. The mixture was extracted with ethyl acetate. The organic phase was washed with water and brine, dried, and stripped. The resulting solid was stirred with 700 mL ethyl acetate for 10 minutes and 2000 mL of heptane was added. This mixture was stirred for 15 minutes and then filtered. The residue was washed with a mixture of 275 mL ethylacetate/825 mL heptane and air dried to give 2,5-Bis(4-(2-ethylhexyl)benzoyl)terephthalic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06974877B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-3ff297a5ecdd4e09a258ec395be42f04
출처 메모uspto-grants-2005_12