HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227202Erstellt: 24. Oktober 2026
Acrylic Acid → N-propan-2-ylprop-2-enamide;prop-2-enoic acid
https://huagongshe.com/de/reaction/227202
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acrylic Acid | HCID 6581 | — |
| Edukt | N-Isopropylacrylamide | HCID 16637 | — |
| Edukt | Potassium Persulfate | HCID 24412 | — |
| Edukt | Sodium Lauryl Sulfate | HCID 3423265 | — |
| Edukt | Methylene-bisacrylamide | HCID 53800990 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-propan-2-ylprop-2-enamide;prop-2-enoic acid | HCID 157470 | — |
Reaktionsschritte
Sodium dodecylsulfate (20 mg), N-isopropylacrylamide (2.7 g), acrylic acid (172 mg), and methylenebisacrylamide (121 mg) are dissolved in 200 ml of water, and, after a 30 minute stirring at 70° C. in a nitrogen atmosphere, a polymerization initiator (potassium persulfate 9.2 mg) is added, followed by 4 hours of stirring. The obtained particles (precursor of Example 1-2) are purified in water by means of dialysis, and then lyophilized. These particles are then dispersed in tetrahydrofuran (30 ml)/dimethylformamide (10 ml), and a tetrahydrofuran (10 ml)/dimethylformamide (50 ml) solution of dicyclohexylcarbodiimide (800 mg), hydroxybenzotriazole (500 mg), and 2,2′-(ethylenedioxy)bis(ethylamine) (1.14 g) is added at room temperature, followed by an overnight stirring. The particles are then dialyzed and lyophilized. Next, they are dispersed in methanol (70 ml), to which 1 g of the chemical compound of Synthetic example 1 is added, followed by a 6 hour stirring at room temperature; this mixture is cooled in an ice bath, 2.8 g of sodium cyanotrihydroborate is added, followed by an overnight stirring at room temperature. The obtained particles are dialyzed in water to obtain the target N-isopropylacrylamide/acrylic acid copolymer particles (620 mg) having phosphorylcholine groups directly on the particle surface.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07560023B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-fdb1c49ab6034e68adfb0fa4e76d350e |
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| Quellennotiz | uspto-grants-2009_07 |
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