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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745024Generated: October 30, 2026

Sodium Iodide → HCID 10055828, compound

https://huagongshe.com/reaction/745024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCarbonic acid, 1-chloroethyl ethyl esterHCID 162095—
Reactantpotassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 23717801—
SolventDimethylformamideHCID 6228—
ProductHCID 10055828HCID 10055828—

Reaction Conditions

Temperature50 °C

Reaction Steps

1-Chloroethyl ethyl carbonate (10.00 g, 66.0 mmol) was added dropwise during 1.5 hour at room temperature to a solution of potassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate (40.00 g, 60.0 mmol) and sodium iodide (0.89 g, 6.0 mmol) in dry dimethylformamide (200 ml). After stirring at 50° C. for 24 hours the solvent was removed at reduced pressure. The residue was dissolved in chloroform (120 ml) and washed four times with a saturated sodium hydrogen carbonate solution and twice with water. After drying with magnesium sulfate, treatment with activated charcoal and filtration, the title compound was crystallised by concentrating the solution at reduced pressure. Yield: (79%). Purity by HPLC: 99%. 1H-NMR (DMSO-d6): delta=1.25 (t, J=7 Hz, CH3); 1.64 (d, J=6 Hz, CH3); 1.67 (s, N(Me)COCH3); 2.05(s, NCOCH3); 2.96 (s, NCH3); 4.21 (q, J=7 Hz, CH2); 6.97 (q, J=6 Hz, CH); 10.10 ppm (s, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559266
Source datasetuspto-grants-1996_09
ORD IDord-d28ab77b63924d79b181bf8dba6a02d9
Source noteuspto-grants-1996_09