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HRID 31408作成日:2026年10月25日

Methanol → 5-(4-Iodophenyl)-3-methyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/31408

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物4-Iodobenzoic acidHCID 12085—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物Sodium MethoxideHCID 10942334—
反応物HCID 178465666HCID 178465666—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物5-(4-Iodophenyl)-3-methyl-1,2,4-oxadiazoleHCID 1970311626%

反応手順

1,1′-Carbonyldiimidazole (0.49 g, 3 mmol) was added to a solution of 4-iodobenzoic acid (0.5 g, 2 mmol) in dry dimethylformamide (4 ml) and stirred at room temperature for 30 minutes. N-hydroxy-acetamidine (0.224 g, 3 mmol) was added and stirring at room temperature continued for 16 hours. Sodium methoxide in methanol (25% wt solution; 1.1 ml, 5 mmol) was added and the mixture heated at 80° C. for 6 hours. Once cool, ethyl acetate (50 ml) and water (50 ml) were added. The organic layer was washed with water (50 ml), brine (50 ml), dried over magnesium sulfate, filtered and solvent removed in vacuo. The residue was purified by silica SPE cartridge (5 g) (100% cyclohexane, 20:1 cyclohexane/ethyl acetate v:v to 10:1 cyclohexane/ethyl acetate v:v) to yield the desired product as a white solid (0.15 g, 0.52 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425555B2
出典データセットuspto-grants-2008_09
ORD IDord-2dc827775f15424f9227b48bef98f4d9
出典メモuspto-grants-2008_09