HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Maleic Anhydride → 6,10-Dihydroxy-4,12-dioctyl-3,13-dioxo-8-sulfoethyl-4,8,12-triaza-1,14-pentadecadiene-1,15-dicarboxylic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | 11,15-Dihydroxy-13-sulfoethyl-9,13,17-triazapentacosane | HCID 54347802 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | 6,10-Dihydroxy-4,12-dioctyl-3,13-dioxo-8-sulfoethyl-4,8,12-triaza-1,14-pentadecadiene-1,15-dicarboxylic acid | HCID 53732392 | 80% |
Reaktionsschritte
A reactor was charged with 20 g (0.04 mole) of 11,15-dihydroxy-13-sulfoethyl-9,13,17-triazapentacosane and 100 g of xylene, to which 10 g (0.1 mole) of maleic anhydride were then added with stirring to conduct a reaction at 50° C. for 6 hours. After xylene was distilled off under reduced pressure, 300 ml of water were added, and 10% sodium hydroxide was further added to keep the pH of the reaction mixture at 7. Thereafter, the reaction mixture was subjected to electrodialysis and lyophilized, thereby obtaining 22 g (isolation yield: 80%) of 6,10-dihydroxy-4,12-dioctyl-3,13-dioxo-8-sulfoethyl-4,8,12-triaza-1,14-pentadecadiene-1,15-dicarboxylic acid as white powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05723655 |
| Quelldatensatz | uspto-grants-1998_03 |
| ORD ID | ord-edde2bbf24c7456a8918ccba8422abf0 |
| Quellennotiz | uspto-grants-1998_03 |