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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1185973Erstellt: 25. Oktober 2026

Acrylic Acid → N-propan-2-ylprop-2-enamide;prop-2-enoic acid

https://huagongshe.com/reaction/1185973

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcrylic AcidHCID 6581—
EduktN-IsopropylacrylamideHCID 16637—
EduktPotassium PersulfateHCID 24412—
EduktSodium Lauryl SulfateHCID 3423265—
EduktMethylene-bisacrylamideHCID 53800990—
LösungsmittelWaterHCID 962—
ProduktN-propan-2-ylprop-2-enamide;prop-2-enoic acidHCID 157470—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Sodium dodecylsulfate (20 mg), N-isopropylacrylamide (2.4 g), acrylic acid (382 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 3) are purified in water by means of dialysis, and then lyophilized. These particles (700 mg) 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. They are dispersed in methanol (70 ml), to which 1.2 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, and 3 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 (650 mg) containing phosphorylcholine groups.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08673151B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-be0d957f7a3a406a9a075510cd26e48c
Quellennotizuspto-grants-2014_03