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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260540생성일: 2026년 10월 26일

4-Pentenoyl chloride → N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-2,4,6-triiodo-5-[(1-oxo-4-pentenyl) amino]-1,3-benzenedicarboxamide

https://huagongshe.com/reaction/260540

반응식

참여 물질

역할이름HCID투입량
반응물4-Pentenoyl chlorideHCID 4228493—
반응물N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)methyl]ethyl]-5-amino-2,4,6-triiodo-1,3-benzenedicarboxamideHCID 11766168—
용매DimethylacetamideHCID 31374—
생성물N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-2,4,6-triiodo-5-[(1-oxo-4-pentenyl) amino]-1,3-benzenedicarboxamideHCID 1037369189%

반응 단계

4-Pentenoyl chloride (11.9 g, 100 mmol) was added to a stirred solution of N,N'-bis-[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-5-amino-2,4,6 -triiodo-1,3-benzenedicarboxamide (47.75 g, 50 mmol) in dimethylacetamide (400 mL) at room temperature and the mixture was stirred for 16 hours. Dimethylacetamide was removed in vacuo and the residue dissolved in ethyl acetate (600 ml). The solution was washed with aqueous sodium bicarbonate (10%, 2×150 mL) and with water (2×100 mL) and brine (150 mL). The organic layer was dried and the solvent removed to obtain the crude product as an off-white solid. Further purification by crystallization from a mixture of acetone (250 mL) and hexane (75 mL) afforded the title A compound (42.5 g), m.p. 162°-64°. TLC: Rf 0.55 in ethyl acetate. Mass Spectrum: m/z 956 (M+H)+, 830, 653.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05527926
출처 데이터셋uspto-grants-1996_06
ORD IDord-a227adb5584347019e9cf0455f838307
출처 메모uspto-grants-1996_06