StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Hydrogen Bromide → Phosphonic acid, (3-bromo-2-hydroxypropyl)-, diethyl ester

HRID 1706176
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1706176
[BrH:1].[O:2]1[CH2:13][CH:3]1[CH2:4][P:5](=[O:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8]>>[Br:1][CH2:13][CH:3]([OH:2])[CH2:4][P:5](=[O:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 260Hydrogen BromideHCID 98446Diethyl 2,3-epoxypropylphosphonate

Produkt 1

HCID 10934659Phosphonic acid, (3-bromo-2-hydroxypropyl)-, diethyl esterAusbeute 86,1 %

Versuchsvorschrift

(1)-(a) 47% Aqueous hydrobromic acid (82.8 g) was added dropwise to diethyl 2,3-epoxypropylphosphonate (77.6 g) under ice-cooling and with stirring over a five minutes interval. After the stirring was continued for an hour under ice-cooling and for 3 hours at ambient temperature, the reaction mixture was extracted with ethyl acetate (500 ml). The ethyl acetate layer was separated, washed three times with saturated aqueous sodium bicarbonate solution (200 ml and 100 ml×2) and twice with saturated aqueous sodium chloride solution (100 ml×2), dried over magnesium sulfate and evaporated to dryness to give oily diethyl 3-bromo-2-hydroxypropylphosphonate (94.7 g)

Aufarbeitung

  • temperaturecooling
  • waitAfter the stirring was continued for an hour under ice-
  • extractionthe reaction mixture was extracted with ethyl acetate (500 ml)
  • customThe ethyl acetate layer was separated
  • washwashed three times with saturated aqueous sodium bicarbonate solution (200 ml and 100 ml×2)
  • dry with materialtwice with saturated aqueous sodium chloride solution (100 ml×2), dried over magnesium sulfate
  • customevaporated to dryness
  • Quellen und Nachweise

    ORD-Eintrag
    ord-e50c9f12300d45b497fb3b4f23662bed
    Quelldatensatz
    uspto-grants-1980_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04206156

    Notizen zur Reaktion

    Wird geladen…

    Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion