Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865618Generated: October 29, 2026

Ethyl Acetate → HCID 18688969, compound

https://huagongshe.com/reaction/865618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide TetraacetateHCID 9897534—
ReactantHCID 15186552HCID 15186552—
SolventDichloromethaneHCID 6344—
ProductHCID 18688969HCID 18688969—

Reaction Steps

5-Amino,N,N'-bis(2,3-diacetoxypropyl)-2,4,6-triiodoisophthalamide (2.19 g, 2.5 mmol) and 10,12-tricosadiynoyl chloride (1.82 g, 5 mmol) were dissolved in 20 ml dichloromethane. The solution was stirred for 3 days at ambient temperature under a nitrogen atmosphere. TLC (ethyl acetate) indicated that the reaction was complete. The reaction mixture was evaporated and dissolved in a mixture of methanol (30 ml) and 1M sodium hydroxide solution (15 ml). After 1 hour TLC (methanol/chloroform) indicated that the reaction was complete. The solution was neutralized with concentrated hydrochloric acid. The residue was dissolved in chloroform and filtered. The solvent was removed and the reaction mixture was purified through silica gel with methanol/chloroform (1:3) to give the title compound. 1H NMR (300 MHz, DMSO): δ 0.8 (CH3, t), 1.2-1.7 (17×CH2, m), 2.2-2.3 (2×CH2, t) , 3.1-3.2 (2×CH2NH, m) , 3.3-3.5 (2×CH2OH, m), 3.6-3.8 (2×CHOH), 4.4-4.7 (4×OH, m), 8.4-8.5 (2×CONH, m), 9.8 (2×ArNHCO, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05567413
Source datasetuspto-grants-1996_10
ORD IDord-2460ec314a0548428ac0ffa1c7157c3b
Source noteuspto-grants-1996_10