Reaktionsgleichung
C([Li])CCC.[CH3:6][Si:7]([C:10]#[CH:11])([CH3:9])[CH3:8].[CH2:12]([O:14][P:15](Cl)[O:16][CH2:17][CH3:18])[CH3:13]>O1CCCC1>[CH3:6][Si:7]([C:10]#[C:11][P:15]([O:16][CH2:17][CH3:18])[O:14][CH2:12][CH3:13])([CH3:9])[CH3:8]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- -20 °C
Versuchsvorschrift
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).
Aufarbeitung
- temperaturewhilst maintaining the temperature below -65° C
- waitAfter twenty minutes
- waitcontinued for a further ninety minutes at -65° C
- customquenched by dropwise addition of saturated ammonium chloride solution (10 ml)
- customto reach room temperature
- additiondiluted with water (10 ml)
- extractionextracted with chloroform (4×25 ml)
- dry with materialThe extracts were dried over magnesium sulphate
- customevaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-01b0f93d550c45e19bf61efdb1888782
- Quelldatensatz
- uspto-grants-1995_02
- Patentnummer
- US05393732
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