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HRID 1973441作成日:2026年10月25日

Potassium Iodide → N-(2-(2-Methyl-5-nitro-1H-imidazol-1-yl)ethyl)phthalimide

https://huagongshe.com/reaction/1973441

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物DimethylformamideHCID 6228—
反応物1-(2-Chloroethyl)-2-methyl-5-nitroimidazoleHCID 83210—
反応物Phthalimide potassium saltHCID 24194345—
溶媒TolueneHCID 1140—
生成物N-(2-(2-Methyl-5-nitro-1H-imidazol-1-yl)ethyl)phthalimideHCID 120116—

反応手順

A mixture of 17.0 parts of 1-(2-chloroethyl)-2-methyl-5-nitroimidazole, 18.0 parts of potassium phthalimide, and 2.0 parts of potassium iodide in 240 parts of dimethylformamide is heated in a boiling water bath for 3 hours with stirring. Stirring is then continued for 16 hours at room temperature. The resulting brown mixture is diluted with 870 parts of toluene and the toluene solution is washed with several portions of water. The toluene solution is dried over sodium sulfate and the solvent is evaporated to leave a residue which is digested with cold alcohol. The alcohol solution is then cooled and the precipitate which forms is separated by filtration and recrystallized from ethanol to give N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]phthalimide melting at about 177° C. This compound has the following formula ##STR6##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03997572
出典データセットuspto-grants-1976_12
ORD IDord-513ccd2c1b85446794e18bd6e223f312
出典メモuspto-grants-1976_12