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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2452생성일: 2026년 10월 23일

Sodium Iodide → 4-[(1,3-dioxoisoindol-2-yl)methyl]-N-(2-methoxyphenyl)benzamide

https://huagongshe.com/ko/reaction/2452

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물PhthalimideHCID 6809—
반응물Sodium hydrideHCID 24758—
반응물4-Chloromethyl-N-(2-methoxyphenyl)benzamideHCID 19689968—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물4-[(1,3-dioxoisoindol-2-yl)methyl]-N-(2-methoxyphenyl)benzamideHCID 299452077.6%

반응 단계

In an atmosphere of argon, phthalimide (150 mg, 1.0 mmol) was dissolved in THF (10 ml) to which was subsequently added sodium hydride (44 mg, 60%, 1.1 mmol) at room temperature. After 40 minutes of stirring at the same temperature, to this was added a DMF solution (5 ml) containing 4-chloromethyl-N-(2-methoxyphenyl)benzamide (276 mg, 1.0 mmol) and a catalytically effective amount of sodium iodide. After 2 hours of stirring at 80° C. and subsequent removal of the solvent by evaporation, the resulting residue was mixed with water (10 ml) and extracted with an ethyl acetate-methylene chloride (1:2) mixture solution. The resulting organic layer was washed with water and saturated brine and dried on anhydrous magnesium sulfate. Thereafter, the solvent was removed by evaporation, and the resulting residue was subjected to a silica gel column chromatography (methylene chloride-ether:hexane=2:1) and then washed with ether to obtain 300 mg (77.6%) of the title compound in the form of colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728835
출처 데이터셋uspto-grants-1998_03
ORD IDord-0629cd8f2ed34187aae991fef93b63da
출처 메모uspto-grants-1998_03