Acetic Acid → Trimethoxysilylpropyldimethylammonium acetate
반응식
[CH3:1][O:2][Si:3]([CH2:8][CH2:9][CH2:10][N:11]([CH3:13])[CH3:12])([O:6][CH3:7])[O:4][CH3:5].[C:14]([OH:17])(=[O:16])[CH3:15]>C(O)C>[C:14]([O-:17])(=[O:16])[CH3:15].[CH3:1][O:2][Si:3]([CH2:8][CH2:9][CH2:10][NH+:11]([CH3:13])[CH3:12])([O:4][CH3:5])[O:6][CH3:7]참가 물질
실험 절차
5.0 g of trimethoxysilylpropyldimethylamine and 24 g of ethanol were charged into a 100 mL flask to be dissolved. While stirring the resultant mixed solution with a magnetic stirrer, to the mixed solution, a solution in which 1.5 g of acetic acid was dissolved in 24 g of ethanol was gradually added at room temperature in a nitrogen atmosphere. The reaction mixture was stirred for half a day and therefrom, ethanol was distilled off under reduced pressure. The resultant concentrate was dropped into 100 mL of diethyl ether and therefrom, trimethoxysilylpropyldimethylamine and acetic acid as by-products were removed. This purification was repeated three times and then remaining diethyl ether was distilled off under reduced pressure, followed by dissolving the resultant concentrate in ethanol to obtain a 13.1% ethanol solution of trimethoxysilylpropyldimethylammonium acetate.
후처리
- dissolutionto be dissolved
- additionmixed solution with a magnetic stirrer
- additionwas gradually added at room temperature in a nitrogen atmosphere
- stirringThe reaction mixture was stirred for half a day
- distillationethanol was distilled off under reduced pressure
- concentrationThe resultant concentrate
- additionwas dropped into 100 mL of diethyl ether
- customtrimethoxysilylpropyldimethylamine and acetic acid as by-products were removed
- customThis purification
- distillationremaining diethyl ether was distilled off under reduced pressure
- dissolutionby dissolving the resultant
- concentrationconcentrate in ethanol
출처 및 근거
- ORD 기록
- ord-cce9d0ec598a43b0b318ccb58cb03573
- 출처 데이터셋
- uspto-grants-2014_10
- 특허 번호
- US08864894B2
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