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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383039Generated: October 26, 2026

Methanol → 5-Amino-3-acetoxymethyl-N-(1,3,4-trihydroxybut-2-yl)-2,4,6-triiodobenzamid

https://huagongshe.com/reaction/383039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium CarbonateHCID 10340—
Reactant6-Amino-2,2-dimethyl-1,3-dioxepan-5-olHCID 3387444—
Reactant5-Amino-3-acetoxymethyl-2,4,6-triiodobenzoyl chlorideHCID 18429338—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-Amino-3-acetoxymethyl-N-(1,3,4-trihydroxybut-2-yl)-2,4,6-triiodobenzamidHCID 1842934399.5%

Reaction Conditions

Temperature65 °C

Reaction Steps

5-Amino-3-acetoxymethyl-2,4,6-triiodobenzoyl chloride (12.0 g, 19.8 mmol) was dissolved in dioxane (40 ml). 6-Amino-2,2-dimethyl-1,3-dioxepane-5-ol (3.20 g, 19.8 mmol) and sodium carbonate (2.10 g, 19.8 mmol) were added and the mixture heated to reflux for 10 h. The reaction mixture was cooled, methanol (100 ml) and water (50 ml) were added and the solution was neutralized with a strongly acidic ion exchange resin. The resin was filtered off and a aqueous solution of hydrochloric acid (2M, 20 ml) was added. The mixture was stirred at 60-70° C. for 30 min, and then evaporated to dryness, which gave a semisolid residue (13.6 g) which was used without further purification in the next steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310243B1
Source datasetuspto-grants-2001_10
ORD IDord-06a19f21bf6248c5bfbfe4c139ba6892
Source noteuspto-grants-2001_10