돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488965생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/488965

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Pyromellitic dianhydrideHCID 6966—
반응물P-XyleneHCID 7809—
반응물DiisopropylethylamineHCID 81531—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,2-DichloroethaneHCID 11—
생성물2,5-Bis(2,5-dimethybenzoyl)terephthalic acidHCID 22561363—

반응 조건

온도15 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06974877B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-1aa852da6f814d4ba199a95f4a4a6096
출처 메모uspto-grants-2005_12