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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650457Generated: October 29, 2026

Potassium Iodide → HCID 21712000, compound

https://huagongshe.com/reaction/650457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantHCID 14593424HCID 14593424—
Reactantpotassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 23717801—
SolventDimethylformamideHCID 6228—
ProductHCID 21712000HCID 21712000—

Reaction Conditions

Temperature50 °C

Reaction Steps

1-Chloroethyl octadecyl carbonate (7.54 g, 20 mmol) was added at room temperature to a solution of potassium 5-acetamido-3-(N-methylacetamido)-2,4,6-triiodobenzenecarboxylate (15.99 g, 24 mmol) and potassium iodide (0.33 g, 2 mmol) in dry N,N-dimethylformamide. After stirring at 50° C. for 18 hours the solvent was removed at reduced pressure. The residue was suspended in chloroform (200 ml) and washed three times with a saturated sodium bicarbonate solution and finally twice with water. After drying with magnesium sulphate the solvent was removed at reduced pressure. Yield: 18.6 g. The product was further purified by flash chromatography (Silicagel 60, chloroform/acetonitrile 85:15). 1H NMR (DMSO-d6): δ 0.852(CH2CH3), 1.236(CH2), 1.639(CHCH3),1.657(COOCH2CH2), 1.670(N(CH3)COCH3), 2.051(NCOCH3),2.965(NCH3), 4.154(COOCH2), 6.971 (CHCH3),10.103 (NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274120B1
Source datasetuspto-grants-2001_08
ORD IDord-341ad26b3aae49799243addef0ca3d96
Source noteuspto-grants-2001_08