Reaktionsgleichung
[OH-].[CH2:2]([N+:18]([CH3:21])([CH3:20])[CH3:19])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].[CH2:22]([O:24][C:25]1[CH:33]=[CH:32][C:28]([C:29]([OH:31])=[O:30])=[C:27]([OH:34])[CH:26]=1)[CH3:23].[OH-].[Na+]>>[CH2:22]([O:24][C:25]1[CH:26]=[C:27]([OH:34])[C:28](=[CH:32][CH:33]=1)[C:29]([O-:31])=[O:30])[CH3:23].[CH2:2]([N+:18]([CH3:21])([CH3:19])[CH3:20])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]Komponenten
4
Versuchsvorschrift
The last third of the cetyl-trimethylammonium hydroxide solution is neutralized with 12.39 g of 4-ethoxy-2-hydroxy-benzoic acid (the equivalent weight of which has been determined as 185.8 by titration with 0.1N sodium hydroxide solution) by scattering in as a powder. The resulting yellow solution in methanol is concentrated to dryness. 31.1 g of a slightly brownish residue are obtained, which can be purified by recrystallization from 300 ml of ethyl acetate several times. Cetyl-trimethylammonium 4-ethoxysalicylate is obtained in (slightly reddish) crystals (titration with perchloric acid in glacial acetic acid gives the expected equivalent weight).
Aufarbeitung
- concentrationThe resulting yellow solution in methanol is concentrated to dryness
- custom31.1 g of a slightly brownish residue are obtained
- customwhich can be purified by recrystallization from 300 ml of ethyl acetate several times
Quellen und Nachweise
- ORD-Eintrag
- ord-f521c99de5604056aadd43cae97847b6
- Quelldatensatz
- uspto-grants-1987_11
- Patentnummer
- US04705860
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