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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280036생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/280036

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Diiodosalicylic acidHCID 8631—
반응물Phosphorus trichlorideHCID 24387—
반응물4-(1-Phenylethenyl)anilineHCID 20040308—
용매DichloromethaneHCID 6344—
용매ChlorobenzeneHCID 7964—
생성물N-[4-(1-phenylethenyl)phenyl]-2-hydroxy-3,5-diiodobenzamideHCID 1360834043.2%

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04587361
출처 데이터셋uspto-grants-1986_05
ORD IDord-9d600bc75a5743b39d2325168a77c40e
출처 메모uspto-grants-1986_05