Trimethyl phosphite → 1,3-Bis(dimethylphosphono)-2-methylene-propane

HRID 1155587Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1155587
[P:1]([O:6]C)([O:4][CH3:5])[O:2][CH3:3].I[CH2:9][C:10]([CH2:12]I)=[CH2:11]>C1C=CC=CC=1>[CH3:3][O:2][P:1]([CH2:9][C:10](=[CH2:11])[CH2:12][P:1]([O:2][CH3:3])([O:4][CH3:5])=[O:6])([O:4][CH3:5])=[O:6]

Komponenten

4

Edukt 2

HCID 8472Trimethyl phosphite2×HCID 110450293-Iodo-2-(iodomethyl)prop-1-ene

Produkt 1

HCID 205268441,3-Bis(dimethylphosphono)-2-methylene-propaneAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

400 ml of trimethyl phosphite was placed into a 2-1 flask equipped with an addition funnel, a gas inlet tube, and a Vigreux column with distilling head. The phosphite was heated at reflux, then a solution of 131 g (0.425 Mole) of 2-iodomethyl-3-iodopropene [see J. Amer. Chem. Soc., 89, 4688 (1967)] in 200 ml of benzene was added dropwise over a period of 2 h, followed by an additional 100 ml of trimethyl phosphite within 30 min. The reaction was run under nitrogen, and approx. 150 ml of distillate was allowed to collect. Distillation of the reaction mixture afforded 106 g (92%) of the title compound, b.p. 125°-7°/0.08 Torr;

Aufarbeitung

  1. customequipped with an addition funnel, a gas inlet tube
  2. distillationa Vigreux column with distilling head
  3. temperatureThe phosphite was heated
  4. temperatureat reflux
  5. customto collect
  6. distillationDistillation of the reaction mixture

Quellen und Nachweise

ORD-Eintrag
ord-508ef7df59f04d7589d21119dff6ea89
Quelldatensatz
uspto-grants-1981_11
Patentnummer
US04302607

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