Reaktion #80446

ord-3480f0481a594e518e4e31c7f928693f

Reaktionsgleichung

O=C([O-])O.[Na+]
NaHCO3
Cl.ClCc1cccnc1
3-picolyl chloride hydrochloride
CCOP(OCC)OCC
triethylphosphite
CCOP(=O)(Cc1cccnc1)OCC
diethyl 3-pyridylmethylphosphonate
Ausbeute 26.2%

Reaktionsbedingungen

Temperatur
85°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe mixture was extracted with CH2Cl2
  2. 2
    TrocknenThe organic phase was dried (MgSO4)
  3. 3
    Einengenconcentrated in vacuo
  4. 4
    TemperaturThe mixture was cooled
  5. 5
    Sonstigepurified by flash column chromotography on silica gel eluting with 5% MeOH

Vorschrift

To a stirred solution of saturated NaHCO3 was added 3-picolyl chloride hydrochloride (8.2 g, 50 mmol). After gas evolution ended, the mixture was extracted with CH2Cl2. The organic phase was dried (MgSO4) and concentrated in vacuo. To the resulting residue was added triethylphosphite (8.3 g, 50 mmol) and the neat mixture was stirred and heated at 85° C. overnight. The mixture was cooled and purified by flash column chromotography on silica gel eluting with 5% MeOH--CH2Cl2 to afford 3.0 g of diethyl 3-pyridylmethylphosphonate as a yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05616596uspto-grants-1997_04