HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383032Generated: October 25, 2026
Acetoxyacetyl chloride → 5-Acetoxyacetamido-3-acetoxymethyl-N-(2,3-diacetoxypropyl)-2,4,6-triiodobenzamide
https://huagongshe.com/reaction/383032
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Acetoxymethyl-5-(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodoaniline | HCID 18429130 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 5-Acetoxyacetamido-3-acetoxymethyl-N-(2,3-diacetoxypropyl)-2,4,6-triiodobenzamide | HCID 18429139 | 100% |
Reaction Steps
5-Amino-3-acetoxymethyl-N-(2,3-diacetoxypropyl)-2,4,6-triiodobenzamide (3.0 g, 4.03 mmol) was dissolved in dry N,N-dimethylacetamide (8 ml) at ambient temperature. With efficient stirring acetoxyacetyl chloride (4.39 ml, 40.3 mmol) was added dropwise, and the mixture was stirred overnight. The mixture was then added slowly with stirring into a saturated solution of sodium hydrogen carbonate (80 ml). The precipitate formed was filtered off and dissolved in chloroform (80 ml). The organic solution was washed with an aqueous saturated solution of NaHCO3 (25 ml), and then evaporated to dryness. The solid residue was dissolved in acetone and filtered through a pad of alumina with acetone as eluent. Evaporation of the solvent gave 3.38 g (100%) of a white crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310243B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-12f0a586f15a42fbaf4c95d7fd23f603 |
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| Source note | uspto-grants-2001_10 |
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