Glycerol → sodium 2-(2,3-Dihydroxypropoxy)ethanesulfonate

HRID 1981

Reaktionsgleichung

Reaktionsgleichung von HRID 1981
[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

7

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

  1. customTo a 500 mL, three neck, round bottom flask equipped with a magnetic stirring bar
  2. distillationClaisen head, condenser (set for distillation)
  3. distillationdistilled from the reaction mixture
  4. temperatureThe solution was cooled to ~100° C. and neutralized to pH 7 with methanesulfonic acid (Aldrich)
  5. customneat material was obtained
  6. 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

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