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HRID 525841作成日:2026年10月26日

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

https://huagongshe.com/reaction/525841

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物(1,1'-Biphenyl)-2-olHCID 7017—
反応物Potassium CarbonateHCID 11430—
反応物1,2-Benzenedicarbonitrile, 3,4,5,6-tetrachloro-HCID 16057—
溶媒Ethyl AcetateHCID 8857—
生成物4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrileHCID 117902707—

反応手順

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:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09341743B2
出典データセットuspto-grants-2016_05
ORD IDord-9f221331d5624b8793ac8825c68b4545
出典メモuspto-grants-2016_05