Reaktion #669350

ord-7bc2622598a14ad295a8c2c5c248b2bc

Reaktionsgleichung

[Li][CH2]CCC
n-Butyllithium
C#C[Si](C)(C)C
trimethylsilylacetylene
CCOP(Cl)OCC
diethylchlorophosphite
CCOP(C#C[Si](C)(C)C)OCC
diethyl trimethylsilylethynylphosphonite

Lösungsmittel

Reaktionsbedingungen

Temperatur
-20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhilst maintaining the temperature below -65° C
  2. 2
    workup.WAITAfter twenty minutes
  3. 3
    workup.WAITcontinued for a further ninety minutes at -65° C
  4. 4
    Sonstigequenched by dropwise addition of saturated ammonium chloride solution (10 ml)
  5. 5
    Sonstigeto reach room temperature
  6. 6
    workup.ADDITIONdiluted with water (10 ml)
  7. 7
    Extraktionextracted with chloroform (4×25 ml)
  8. 8
    TrocknenThe extracts were dried over magnesium sulphate
  9. 9
    Sonstigeevaporated under reduced pressure

Vorschrift

n-Butyllithium (26.02 ml, 1.55M in hexane) was added dropwise over thirty minutes to a stirred solution of trimethylsilylacetylene (5.18 ml) in dry tetrahydrofuran (25 ml), whilst maintaining the temperature below -65° C. After twenty minutes, diethylchlorophosphite (4.71 ml) was added dropwise over twenty minutes, then stirring continued for a further ninety minutes at -65° C. The stirred mixture was allowed to warm to -20° C., quenched by dropwise addition of saturated ammonium chloride solution (10 ml), then allowed to reach room temperature, diluted with water (10 ml) and extracted with chloroform (4×25 ml). The extracts were dried over magnesium sulphate and evaporated under reduced pressure to give diethyl trimethylsilylethynylphosphonite as a brown oil (7.34 g, 83% pure by GC).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05922644uspto-grants-1999_07