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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31408생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/31408

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물4-Iodobenzoic acidHCID 12085—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Sodium MethoxideHCID 10942334—
반응물HCID 178465666HCID 178465666—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물5-(4-Iodophenyl)-3-methyl-1,2,4-oxadiazoleHCID 1970311626%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425555B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-2dc827775f15424f9227b48bef98f4d9
출처 메모uspto-grants-2008_09