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HRID 280037作成日:2026年10月26日

3,5-Diiodosalicylic acid → N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamide

https://huagongshe.com/reaction/280037

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Diiodosalicylic acidHCID 8631—
反応物Phosphorus trichlorideHCID 24387—
反応物1-(4-Amino-2-chloro-6-methylphenyl)-1-(4-chlorophenyl)ethyleneHCID 23323150—
生成物N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamideHCID 23323149—

反応手順

Using the reaction sequence of Example 4, 3,5-diiodosalicylic acid is reacted with 1-(4-amino-2-chloro-6-methylphenyl)-1-(4-chlorophenyl)ethylene in the presence of phosphorus trichloride to give N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamide. The benzophenone used as starting material for the Wittig reaction was prepared by reacting 4-chlorobenzyl cyanide with 3-chloro-5-methyl-1-nitrobenzene followed by oxidation with alkaline peroxide as known in the literature.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04587361
出典データセットuspto-grants-1986_05
ORD IDord-91459bcd657c4ad9b89aeb1ee04995d5
出典メモuspto-grants-1986_05