Reaktionsgleichung
[PH2:1](=[O:3])[O-:2].[NH4+].C[Si](C)(C)N[Si](C)(C)C.[CH2:14](Cl)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>ClCCl>[CH2:14]([PH:1](=[O:2])[O:3][CH2:14][CH2:15][CH2:16][CH3:17])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 110 °C
Versuchsvorschrift
A mixture of ammonium phosphinate (9.18 g) and hexamethyldisilazane (25 mL) was heated at 110° C. for 2 hours. The mixture was cooled in ice, dissolved in dry dichloromethane (120 mL), benzyl chloride (20 g; 14 mL) was added and the mixture allowed to warm to room temperature and stirred 18 hours. The solution was filtered, the solvent evaporated, the residue azeotroped with methanol (2×70 mL), dissolved in toluene (150 mL) containing n-butanol (30 mL) and the solution was boiled under reflux in a Dean and Stark water trap for 5 hours. The solvent was evaporated, the residue slurried with dichloromethane (120 mL), filtered and evaporated and the residue chromatographed on silica-gel in 1-2% methanol in dichloromethane to give the title compound as an oil.
Aufarbeitung
- temperatureThe mixture was cooled in ice
- temperatureto warm to room temperature
- filtrationThe solution was filtered
- customthe solvent evaporated
- customthe residue azeotroped with methanol (2×70 mL)
- dissolutiondissolved in toluene (150 mL)
- additioncontaining n-butanol (30 mL)
- temperatureunder reflux in a Dean and Stark water trap for 5 hours
- customThe solvent was evaporated
- filtrationfiltered
- customevaporated
- customthe residue chromatographed on silica-gel in 1-2% methanol in dichloromethane
Quellen und Nachweise
- ORD-Eintrag
- ord-fbb7b4f2d98e40cc842d6d8dc54f1727
- Quelldatensatz
- uspto-grants-1998_03
- Patentnummer
- US05726165
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