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HRID 2452作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物PhthalimideHCID 6809—
反応物Sodium hydrideHCID 24758—
反応物4-Chloromethyl-N-(2-methoxyphenyl)benzamideHCID 19689968—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物4-[(1,3-dioxoisoindol-2-yl)methyl]-N-(2-methoxyphenyl)benzamideHCID 299452077.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728835
出典データセットuspto-grants-1998_03
ORD IDord-0629cd8f2ed34187aae991fef93b63da
出典メモuspto-grants-1998_03