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HRID 227205作成日:2026年10月26日

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

https://huagongshe.com/reaction/227205

反応式

関与物質

役割名称HCID仕込み量
反応物Acrylic AcidHCID 6581—
反応物N-IsopropylacrylamideHCID 16637—
反応物Potassium PersulfateHCID 24412—
反応物Sodium Lauryl SulfateHCID 3423265—
反応物Methylene-bisacrylamideHCID 53800990—
溶媒WaterHCID 962—
生成物N-propan-2-ylprop-2-enamide;prop-2-enoic acidHCID 157470—

反応条件

温度70 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560023B2
出典データセットuspto-grants-2009_07
ORD IDord-c4b5cd0e365649caba71cfcaf7dc5d51
出典メモuspto-grants-2009_07