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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 525841생성일: 2026년 10월 25일

Acetonitrile → 4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrile

https://huagongshe.com/reaction/525841

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물(1,1'-Biphenyl)-2-olHCID 7017—
반응물Potassium CarbonateHCID 11430—
반응물1,2-Benzenedicarbonitrile, 3,4,5,6-tetrachloro-HCID 16057—
용매Ethyl AcetateHCID 8857—
생성물4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrileHCID 117902707—

반응 단계

To a 250 mL flask, 4.8 g of tetrachlorophthalonitrile, 4.3 g of biphenyl-2-ol, 5 g of potassium carbonate (K2CO3) and 55 mL of acetonitrile are added, followed by heating for 12 hours while refluxing. After completion of the reaction, 30 mL of ethyl acetate is added and filtered to remove the solvent. To the obtained solid, a suitable amount of dichloromethane is added to dissolve the solid, followed by adding hexane for crystallization. The obtained solid is filtered and dried under vacuum to obtain a compound, 4-[(biphenyl-2-yl)oxy]-3,5,6-trichlorophthalonitrile. The second step reaction may be represented by Reaction Scheme 2:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09341743B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-9f221331d5624b8793ac8825c68b4545
출처 메모uspto-grants-2016_05