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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260540Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Pentenoyl chlorideHCID 4228493—
ReactantN,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)methyl]ethyl]-5-amino-2,4,6-triiodo-1,3-benzenedicarboxamideHCID 11766168—
SolventDimethylacetamideHCID 31374—
ProductN,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-2,4,6-triiodo-5-[(1-oxo-4-pentenyl) amino]-1,3-benzenedicarboxamideHCID 1037369189%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527926
Source datasetuspto-grants-1996_06
ORD IDord-a227adb5584347019e9cf0455f838307
Source noteuspto-grants-1996_06