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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491526Generated: October 27, 2026

Sodium Iodide → 1-(Phenyloxycarbonyloxy)-1-phenylmethyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate

https://huagongshe.com/reaction/1491526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactantpotassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 23717801—
Reactant1-Chloro-1-phenylmethyl phenyl carbonateHCID 54216522—
SolventDimethylformamideHCID 6228—
Product1-(Phenyloxycarbonyloxy)-1-phenylmethyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 53992708—

Reaction Conditions

Temperature60 °C

Reaction Steps

1-Chloro-1-phenylmethyl phenyl carbonate (0.63 g, 2.4 mmol) was added at room temperature to a solution of potassium 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate (1.44 g, 2.2 mmol) and sodium iodide (0. 034 g, 0.23 mmol) in dry DMF (12 ml). After stirring at 60° C. for 2 hours and at room temperature for 18 hours the solvent was removed at reduced pressure. The residue was suspended in chloroform (20 ml) and washed four times with a saturated sodium hydrogen carbonate solution and finally twice with water. After drying with magnesium sulfate the solution was evaporated to dryness. Yield: 0.90 g. Purity by HPLC: 96.6 % 1H-NMR (DMSO-d6): delta=1.67 (NCH3COCH3); 2.05 (NHCOCH3); 2.96 (NCH3); 7.29-7.54 phenyl); 7.71 (CH); 10.13 ppm (NH) . FAB/MS: 854 (M+) .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05370861
Source datasetuspto-grants-1994_12
ORD IDord-d50f006aba2944cc9e4a20bbb80ec33a
Source noteuspto-grants-1994_12