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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1158210생성일: 2026년 10월 27일

Dichloromethane → [3,5-Bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanone

https://huagongshe.com/reaction/1158210

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물FluorobenzeneHCID 10008—
반응물Trimesoyl chlorideHCID 78138—
반응물Aluminum(III) ChlorideHCID 6451240—
용매WaterHCID 962—
생성물[3,5-Bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanoneHCID 330233970%

반응 조건

온도25 °C

반응 단계

5 g of 1,3,5-benzenetricarbonyltrichloride (18.8 mol), 6.7 g of aluminum chloride (50.0 mmol) and 50 mL of distilled dichloromethane (DCM) were put in a 250 mL round flask, which was stirred for 30 minutes at 25° C. for reaction in the presence of nitrogen. 20 mL of dichloromethane and 4.5 g of fluorobenzene (48.8 mmol) were added in 100 mL of Dropping funnel, and the fluorobenzene solution was dropped in the round flask drop by drop. The reaction mixture was stirred for 4 hours in the presence of nitrogen, to which 20 mL of distilled water was added. The reaction mixture was stirred further for more than 12 hours. The organic layer of the reaction mixture was extracted by using dichloromethane, and the organic solvent was eliminated, resulting in a crude product. The crude product was re-crystallized using ethanol to give white brancher [3,5-bis(4-fluorobenzoyl)phenyl](4-fluorophenyl) methanone (yield: 70%). The structure of the [3,5-bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanone was confirmed by 1H-NMR, 13C-NMR spectrometry and elemental analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07807759B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-042bf47390bb40fd83c61f958c290906
출처 메모uspto-grants-2010_10