Reaktion #461416

ord-dc1cc74ee0e64fada48665083944095b

Reaktionsgleichung

[Al+3].[H-].[H-].[H-].[H-].[Li+]
LiAlH4
COC(=O)c1ccc(-c2ccc(C(=O)OC)cc2)cc1
4,4'-bis (methoxycarbonyl)biphenyl
OCc1ccc(-c2ccc(CO)cc2)cc1
4,4'-bis (hydroxymethyl) biphenyl
Ausbeute 96.7%

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheating bath
  2. 2
    workup.ADDITIONis added dropwise, over a period of 1 hour, to the mixture
  3. 3
    Temperaturthe mixture is cooled to ambient temperature
  4. 4
    Sonstigethe excess LiAlH4 is destroyed by the careful addition of 15 ml of a THF/H2O (80:20) mixture
  5. 5
    FiltrationThe reaction mixture is filtered on Septum G2
  6. 6
    Waschenwashing the precipitate with anydrous ethanol (3×100 ml)
  7. 7
    SonstigeThe combined filtrate and washings are evaporated to dryness under vacuum with the heating bath at 40° C
  8. 8
    workup.DISSOLUTIONThe residue is then redissolved with 100 ml of hot acetone (50° C.)
  9. 9
    Filtrationby filtration
  10. 10
    Trocknendried on anhydrous Na2SO4
  11. 11
    Sonstigeevaporated 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%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05166380uspto-grants-1992_11