HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650457Generated: October 29, 2026
Potassium Iodide → HCID 21712000, compound
https://huagongshe.com/reaction/650457
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | HCID 14593424 | HCID 14593424 | — |
| Reactant | potassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate | HCID 23717801 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21712000 | HCID 21712000 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06274120B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-341ad26b3aae49799243addef0ca3d96 |
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| Source note | uspto-grants-2001_08 |
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