HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383039Erstellt: 24. Oktober 2026
Methanol → 5-Amino-3-acetoxymethyl-N-(1,3,4-trihydroxybut-2-yl)-2,4,6-triiodobenzamid
https://huagongshe.com/de/reaction/383039
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 6-Amino-2,2-dimethyl-1,3-dioxepan-5-ol | HCID 3387444 | — |
| Edukt | 5-Amino-3-acetoxymethyl-2,4,6-triiodobenzoyl chloride | HCID 18429338 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 5-Amino-3-acetoxymethyl-N-(1,3,4-trihydroxybut-2-yl)-2,4,6-triiodobenzamid | HCID 18429343 | 99,5% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06310243B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-06a19f21bf6248c5bfbfe4c139ba6892 |
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| Quellennotiz | uspto-grants-2001_10 |
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