HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 518910Erstellt: 25. Oktober 2026
Ethyl isocyanatoacetate → Dihexyl aspartate carbamate
https://huagongshe.com/reaction/518910
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl isocyanatoacetate | HCID 76283 | — |
| Edukt | HCID 86656430 | HCID 86656430 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | N,N-dimethylformamide; methylsulfinylmethane | HCID 3013483 | — |
| Produkt | Dihexyl aspartate carbamate | HCID 86656429 | — |
Reaktionsschritte
2.7 g (i.e., 50 mmol of hydroxyls) of dextran with a weight-average molar mass of approximately 10 kg/mol (Bachem) are dissolved in a DMF/DMSO mixture. The mixture is brought to 130° C. with stirring and 3.2 g (25 mmol) of ethyl isocyanatoacetate and then 3.9 g (8 mmol) of dihexyl 2-isocyanatobutanedioate are gradually introduced. After reacting for 1 h, the medium is diluted in water and purified by diafiltration through a 5 kD PES membrane against 0.1N NaOH, 0.9% NaCl and water. The final solution is quantitatively determined by dry extract, in order to determine the concentration of polymer. A fraction of solution is lyophilized and analyzed by 1H NMR in D2O in order to determine the degree of conversion of the hydroxyls to N-(sodium methylcarboxylate) carbamate and the degree of the functionalization of the hydroxyls to give dihexyl aspartate carbamate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09115218B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-17fc1b3fe5f0430aa9b1b5535a8d6449 |
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| Quellennotiz | uspto-grants-2015_08 |
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