Reaktion #461416
ord-dc1cc74ee0e64fada48665083944095b
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturheating bath
- 2workup.ADDITIONis added dropwise, over a period of 1 hour, to the mixture
- 3Temperaturthe mixture is cooled to ambient temperature
- 4Sonstigethe excess LiAlH4 is destroyed by the careful addition of 15 ml of a THF/H2O (80:20) mixture
- 5FiltrationThe reaction mixture is filtered on Septum G2
- 6Waschenwashing the precipitate with anydrous ethanol (3×100 ml)
- 7SonstigeThe combined filtrate and washings are evaporated to dryness under vacuum with the heating bath at 40° C
- 8workup.DISSOLUTIONThe residue is then redissolved with 100 ml of hot acetone (50° C.)
- 9Filtrationby filtration
- 10Trocknendried on anhydrous Na2SO4
- 11Sonstigeevaporated to dryness
Vorschrift
789 mg (20.8 mmoles) of LiAlH4 in 150 ml of anhydrous THF (tetrahydrofuran) are placed in a 2-liter flask which has a mechanical agitator, cooler, filler funnel and heating bath. A solution, heated to 50° C., of 7.5 g (27.7 mmoles) of 4,4'-bis (methoxycarbonyl)biphenyl in 500 ml of anhydrous THF is added dropwise, over a period of 1 hour, to the mixture, heated in an inert atmosphere to 50° C. under agitation. After a further 30 minutes of agitation in a heating bath, the mixture is cooled to ambient temperature and the excess LiAlH4 is destroyed by the careful addition of 15 ml of a THF/H2O (80:20) mixture. The reaction mixture is filtered on Septum G2, washing the precipitate with anydrous ethanol (3×100 ml). The combined filtrate and washings are evaporated to dryness under vacuum with the heating bath at 40° C. The residue is then redissolved with 100 ml of hot acetone (50° C.), eliminating the insoluble residue by filtration, dried on anhydrous Na2SO4 and evaporated to dryness. 5.74 g of 4,4'-bis (hydroxymethyl) biphenyl are obtained with a molar yield of 96.6%.