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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1280173생성일: 2026년 10월 26일

Acetonitrile → 5-Amino-3-acetoxymethyl-N,N-bis-(2,3-dihydroxypropyl)-2,4,6-triiodo-benzamide

https://huagongshe.com/reaction/1280173

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참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물3,3'-Iminobispropane-1,2-diolHCID 18403554—
반응물5-Amino-3-acetoxymethyl-2,4,6-triiodobenzoyl chlorideHCID 18429338—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물5-Amino-3-acetoxymethyl-N,N-bis-(2,3-dihydroxypropyl)-2,4,6-triiodo-benzamideHCID 1842933193%

반응 조건

온도90 °C

반응 단계

5-Amino-3-acetoxymethyl-2,4,6-triiodobenzoyl chloride (19.9 g, 32.9 mmol) was dissolved in dioxane (45 ml) and triethylamine (3.32 g, 32.9 mmol) was added. To this solution was added bis-(2,3-dihydroxypropyl)amine (5.43 g, 32.9 mmol), and the mixture was stirred at 90° C. for 17 h. After cooling to room temperature, acetonitrile (150 ml), water (70 ml), and a strongly acidic ion exchange resin (Amberlyst 15, 60 g) were added to bring the pH to 4. After stirring at room temperature for 20 min, the resin was filtered off and the filtrate was evaporated to dryness. The semicrystalline dark residue was filtered through a short column of silica using a mixture of methylene chloride and methanol (70/30) as the eluent. The solvent was evaporated and 22.4 g (93%) of a tan coloured crystalline product was obtained. This product was acetylated without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06448442B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-2d71ad42d9b54dce98042a53053e360b
출처 메모uspto-grants-2002_09