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HRID 280036作成日:2026年10月26日

3,5-Diiodosalicylic acid → N-[4-(1-phenylethenyl)phenyl]-2-hydroxy-3,5-diiodobenzamide

https://huagongshe.com/reaction/280036

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4-(1-Phenylethenyl)anilineHCID 20040308—
溶媒DichloromethaneHCID 6344—
溶媒ChlorobenzeneHCID 7964—
生成物N-[4-(1-phenylethenyl)phenyl]-2-hydroxy-3,5-diiodobenzamideHCID 1360834043.2%

反応手順

To a refluxing solution of 7.9 g (0.02 mole) of 3,5-diiodosalicylic acid and 4.6 g (0.02 mole) of 1-(4-aminophenyl)-1-phenylethylene in 125 ml of chlorobenzene was added 3 g (0.022 mole) of phosphorus trichloride over a 1 hour period. The resulting mixture was refluxed for 2 hours, cooled, diluted with 100 ml of methylene chloride. The organic phase was washed with 250 ml of water and dried. The extract was evaporated to dryness. After redissolving the residue in minimum amount of methylene chloride, the solution was flash-chromatographed on a silica gel column. The desired component was eluted with 2 liters of methylene chloride/n-hexane. Evaporation of its solvent gave 4.9 g of N-[4-(1-phenylethenyl)phenyl] -2-hydroxy-3,5-diiodobenzamide. Recrystallization from aqueous ethanol gave 4.2 g of purified product, m.p. 173°-174°.

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-9d600bc75a5743b39d2325168a77c40e
出典メモuspto-grants-1986_05