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Sodium hydride → Tetraethyl (phenoxymethylene)-bisphosphonate

HRID 569603
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 569603
[CH2:1]([O:3][P:4]([O-:8])[O:5][CH2:6][CH3:7])[CH3:2].[H-].[Na+].[C:11]1([O:17][CH:18](Cl)Cl)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>CN(C)C=O.O>[O:17]([CH:18]([P:4](=[O:8])([O:5][CH2:6][CH3:7])[O:3][CH2:1][CH3:2])[P:4](=[O:8])([O:5][CH2:6][CH3:7])[O:3][CH2:1][CH3:2])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 24758Sodium hydrideHCID 319898Dichloromethyl phenyl etherHCID 3780918Diethylphosphite

Produkt 1

HCID 54483224Tetraethyl (phenoxymethylene)-bisphosphonate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6228Dimethylformamide
Lösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Diethylphosphite (20.6 ml) was added dropwise at 20° C. to a stirred suspension of 55% sodium hydride (6.24 g) in dimethylformamide (90 ml). After stirring for a further 15 minutes, the mixture was cooled to 0° C., and dichloromethyl phenyl ether (9.27 g) was added dropwise. Stirring was continued overnight at 45° C., and the mixture was cooled in ice, diluted with water, neutralized and extracted with ethyl acetate. The organic phase was washed repeatedly with water, dried and evaporated in vacuo to yield an oil which was purified by chromatography on silica gel. Eluent: ether-acetone 85:15. The pure title compound was obtained as a colourless oil.

Aufarbeitung

  1. stirringStirring
  2. waitwas continued overnight at 45° C.
  3. temperaturethe mixture was cooled in ice
  4. extractionextracted with ethyl acetate
  5. washThe organic phase was washed repeatedly with water
  6. customdried
  7. customevaporated in vacuo
  8. customto yield an oil which
  9. customwas purified by chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-ddd21daf02a64cb48d14aab9fefdbfa2
Quelldatensatz
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04732998

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