Reaktionsgleichung
[S:1]([CH2:5][CH2:6][OH:7])([OH:4])(=[O:3])=[O:2].[Na].[OH-].[Na+:10].[OH:11][CH2:12][CH:13]([CH2:15]O)[OH:14].P([O-])([O-])([O-])=O.[K+].[K+].[K+]>O>[OH:14][CH:13]([CH2:12][OH:11])[CH2:15][O:7][CH2:6][CH2:5][S:1]([O-:4])(=[O:3])=[O:2].[Na+:10]Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 200 °C
Versuchsvorschrift
To a 500 mL, three neck, round bottom flask equipped with a magnetic stirring bar, modified Claisen head, condenser (set for distillation), thermometer, and temperature controller (Therm-O-Watch®, I2R) was added isethionic acid, sodium salt (Aldrich, 50.0 gm, 0.338 mol), sodium hydroxide (2.7 g, 0.0675 mol), and glycerin (Baker, 310.9 gm, 3.38 mol). The solution was heated at 190° C. under argon overnight as water distilled from the reaction mixture. A 13C-NMR(DMSO-d6) showed that the reaction was complete by the virtual disappearance of the isethionate peaks at ~53.5 ppm and ~57.4 ppm, and the emergence of product peaks at ~51.4 ppm (--CH2SO3Na) and ~67.5 ppm (CH2CH2SO3Na). The solution was cooled to ~100° C. and neutralized to pH 7 with methanesulfonic acid (Aldrich). The desired, neat material was obtained by adding 0.8 mol % of potassium phosphate, monobasic and heating on a Kugelrohr apparatus (Aldrich) at 200° C. for ~3 hr. at ~1 mm Hg to afford 77 gm of yellow waxy solid.
Aufarbeitung
- customTo a 500 mL, three neck, round bottom flask equipped with a magnetic stirring bar
- distillationClaisen head, condenser (set for distillation)
- distillationdistilled from the reaction mixture
- temperatureThe solution was cooled to ~100° C. and neutralized to pH 7 with methanesulfonic acid (Aldrich)
- customneat material was obtained
- customat ~1 mm Hg to afford 77 gm of yellow waxy solid
Quellen und Nachweise
- ORD-Eintrag
- ord-19b4002a336d4a0c990cd5217402dc7e
- Quelldatensatz
- uspto-grants-1998_03
- Patentnummer
- US05728671
Verknüpfte Notizen
Wird geladen…