Hydrochloric Acid → Imidazolium Methanesulfonate

HRID 537699

반응식

HRID 537699 반응식
C1([Si](OC)(OC)OC)C=CC=CC=1.C(O[Si](OCC)(OCC)OCC)C.C[Si](OCC)(OCC)OCC.[CH3:38][S:39]([O-:42])(=[O:41])=[O:40].C(O[Si](CCC[N+:56]1[CH2:60][CH2:59][N:58](C)[CH:57]=1)(OCC)OCC)C.Cl.C(OCC(O)C)C>O.CC(C)=O.CO.C(O)C>[CH3:38][S:39]([O-:42])(=[O:41])=[O:40].[NH+:56]1[CH:60]=[CH:59][NH:58][CH:57]=1

참가 물질

11

실험 절차

4.92 g of phenyltrimethoxysilane, 72.40 g of tetraethoxysilane, 22.04 g of methyltriethoxysilane, 0.64 g of the 30% ethanol solution of triethoxysilylpropyl-3-methyl-4,5-dihydroimidazolium methanesulfonate, and 150 g of acetone were charged into a 500 mL flask to be dissolved and the resultant mixed solution was warmed while stirring the mixed solution with a magnetic stirrer to reflux. Next, 33.10 g of 0.01 M hydrochloric acid was added to the mixed solution. The mixed solution was subjected to the reaction for 240 minutes and then the resultant reaction solution was cooled down to room temperature. Then, 200 g of propylene glycol monoethyl ether was added to the reaction solution, and ethanol and methanol as reaction by-products, acetone, water, and hydrochloric acid were distilled off under reduced pressure to obtain a hydrolysis-condensation product. The polymer thus obtained corresponded to Formula (VII-13):

후처리

  1. dissolutionto be dissolved
  2. additionthe resultant mixed solution
  3. temperaturewas warmed
  4. temperatureto reflux
  5. customThe mixed solution was subjected to the reaction for 240 minutes
  6. customthe resultant reaction solution
  7. distillationwere distilled off under reduced pressure
  8. customto obtain a hydrolysis-condensation product
  9. customThe polymer thus obtained

출처 및 근거

ORD 기록
ord-9f76f36755314092a41ab1e91a95b9f6
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08864894B2

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