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Ethylene Oxide → Sodium butylglyceryl phosphate

HRID 648786
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 648786
[P:1]([O-:9])([O-:8])([O:3][CH2:4][CH2:5][CH2:6][CH3:7])=[O:2].[OH-].[Na+:11].C1[O:14][CH:13]1[CH2:15][OH:16].O1C[CH2:18]1>>[P:1]([O-:9])([O-:8])([O:3][CH:4]([CH2:5][CH2:6][CH2:7][CH3:18])[CH:13]([CH2:15][OH:16])[OH:14])=[O:2].[Na+:11].[Na+:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 6354Ethylene OxideHCID 11164GlycidolHCID 14798Sodium HydroxideHCID 12691398Butyl phosphate

Produkt 1

HCID 86742086Sodium butylglyceryl phosphateAusbeute 81,5 %

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

20 g (0.13 moles) of monobutyl phosphate having a purity of 99% (AV1=360.6, AV2=721.3) was charged into a reactor, to which 129 ml of 1N sodium hydroxide aqueous solution was added and agitated, followed by heating to 70° C. to make a uniform system. At this moment, the acid value of the reaction system was 46.7. While keeping the reaction system at 70° C., 42.7 g of glycidol (the oxirane value=683.7) was gradually dropped, followed by agitation at the temperature for 6 hours, at which the acid value of the reaction system was approximately zero, revealing that the conversion of phosphoric monoester was almost 100%. The reaction product was isolated from the reaction solution by HPLC and the solvent was distilled off under reduced pressure, thereby obtaining 26.5 g of sodium butylglyceryl phosphate (yield: 81.5%).

Aufarbeitung

  1. additionwas added
  2. customat 70° C.
  3. customThe reaction product was isolated from the reaction solution by HPLC
  4. distillationthe solvent was distilled off under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-3db805d76fdb4eebb2993f81287c1e0f
Quelldatensatz
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04736051

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