Reaktion #11284
ord-b216441cd7154d13b5ba6ea06150db8a
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.WAITwas continued at −78° C. for an hour
- 2workup.WAITat −50° C. for an hour
- 3TemperaturThe temperature was maintained at −78° C. for three hours
- 4SonstigeThe cooling bath was removed
- 5workup.WAITthe reaction left
- 6Temperaturto warm to room temperature
- 7workup.ADDITIONThe reaction mixture was poured into saturated ammonium acetate
- 8Extraktionextracted with ether
- 9TrocknenThe ether layer was dried over magnesium sulfate
- 10Einengenconcentrated
- 11Sonstigeto give a viscous oil
- 12SonstigePurification
- 13Temperaturby column chromatography (silica gel eluting with hexane:toluene mixtures of increasing gradient from 100% hexane to 40% hexane)
Vorschrift
n-Butyllithium was added dropwise via syringe to a −78° C. (acetone-dry ice cooling bath) solution of 4-bromo-N,N-diphenylaniline (24 g, 0.074 mole) in 175 ml dry THF. Stirring was continued at −78° C. for an hour and then at −50° C. for an hour. The mixture was cooled to −78° C. and 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (17.22 g, 0.0925 mole) added via syringe in one portion. The temperature was maintained at −78° C. for three hours. The cooling bath was removed and the reaction left to warm to room temperature while standing for 12 hours. The reaction mixture was poured into saturated ammonium acetate and extracted with ether. The ether layer was dried over magnesium sulfate and concentrated to give a viscous oil. Purification by column chromatography (silica gel eluting with hexane:toluene mixtures of increasing gradient from 100% hexane to 40% hexane) gave N,N-diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline as an oil (19.9 g, 72.8% yield), which slowly crystallized to a solid on standing.