돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2188499생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2188499

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Sodium HydroxideHCID 14798—
반응물Senecioic acid amideHCID 20560—
반응물Ammonium PersulfateHCID 62648—
반응물2-Acrylamido-2-methyl-1-propanesulfonic acidHCID 65360—
반응물EmulphorHCID 5364713—
반응물Methylene-bisacrylamideHCID 53800990—
반응물HCID 178435162HCID 178435162—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매HexaneHCID 8058—
생성물N,N-Dimethylacrylamide 2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium SaltHCID 87703436—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08323629B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-aa1b19d1538645b3bddf7cf3837b6d6d
출처 메모uspto-grants-2012_12