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HRID 2188499作成日:2026年10月26日

Nitrogen → N,N-Dimethylacrylamide 2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium Salt

https://huagongshe.com/reaction/2188499

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Sodium HydroxideHCID 14798—
反応物Senecioic acid amideHCID 20560—
反応物Ammonium PersulfateHCID 62648—
反応物2-Acrylamido-2-methyl-1-propanesulfonic acidHCID 65360—
反応物EmulphorHCID 5364713—
反応物Methylene-bisacrylamideHCID 53800990—
反応物HCID 178435162HCID 178435162—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
生成物N,N-Dimethylacrylamide 2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium SaltHCID 87703436—

反応手順

Firstly, 35 g of dimethylacrylamide (manufactured by Kojin Co., Ltd.), 17.5 g of 2-acrylamido-2-methylpropanesulfonic acid (manufactured by Sigma), and 7 mg of methylenebisacrylamide were dissolved in ion-exchanged water, and the pH value of the resulting solution was adjusted at 7.0 by the addition of sodium hydroxide. Thereafter, 260 g of n-hexane, 8.7 g of polyoxyethylene (3) oleyl ether (EMULEX 503, manufactured by Nihon Emulsion Co., Ltd.), and 17.6 g of polyoxyethylene (6) oleyl ether (EMULEX 506, manufactured by Nihon Emulsion Co., Ltd.) were introduced into a 1,000 ml three-neck flask provided with a reflux device, were mixed together, and were thus subjected to dissolution. The inside atmosphere of the three-neck flask was then replaced by an N2 gas. The aqueous monomer solution having been prepared in the manner described above was then introduced into the three-neck flask. The resulting mixture was heated to a temperature of 65° C. to 70° C. in an oil bath, while the mixture was being stirred under the N2 gas atmosphere. At the stage at which the system had reached the temperature of 65° C. to 70° C., it was confirmed that the system had come into a semitransparent microemulsion state, and 2 g of ammonium persulfate was then added to the polymerization system. Polymerization was thus begun. The polymerization system was kept at the temperature of 65° C. to 70° C. with stirring, and a microgel was thus formed. After the polymerization had finished, acetone was added to the microgel suspension, and the microgel was thus precipitated. Subsequently, washing with acetone was performed three times, and the residual monomers and the surfactants were thus removed. The obtained precipitate was collected by filtration and dried under reduced pressure, and a white powder-like microgel dry product was thereby obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08323629B2
出典データセットuspto-grants-2012_12
ORD IDord-aa1b19d1538645b3bddf7cf3837b6d6d
出典メモuspto-grants-2012_12