Reaktion #1583878

ord-c5b4b4af12be43909fb27b62397ea093

Reaktionsgleichung

CO
methanol
CC(C)[CH2][Al+][CH2]C(C)C.[H-]
diisobutylaluminum hydride
COC(=O)C(c1ccccc1)c1ccccc1
methyl 2,2-diphenylacetate
[Na+].[OH-]
sodium hydroxide
OCC(c1ccccc1)c1ccccc1
2,2-diphenyl ethanol
Ausbeute 92.4%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter the completion of dropwise addition
  2. 2
    SonstigeAfter the completion of reaction
  3. 3
    Sonstigeat −20° C
  4. 4
    SonstigeAfter the completion of reaction
  5. 5
    Extraktionfor extraction
  6. 6
    WaschenThe organic phase was washed with water
  7. 7
    Trocknendried over anhydrous sodium sulfate
  8. 8
    Sonstigeevaporated
  9. 9
    Sonstigeto remove the solvent

Vorschrift

To a 500 mL three-opening flask was slowly added a solution of diisobutylaluminum hydride in toluene (282 mL, 1 mol/L) at −30° C. After stirring, to the resulting mixture was slowly added a solution of methyl 2,2-diphenylacetate (21 g, 92.8 mmol) in dichloromethane dropwisely. After the completion of dropwise addition, the reaction was conducted at 25° C. for 12 hours. After the completion of reaction monitored by TLC, to the resulting mixture was slowly added methanol (10 mL), dichloromethane (100 mL) and an aqueous sodium hydroxide solution (100 mL, 1 mol/L) at −20° C. After the completion of reaction, to the reaction solution was added dichloromethane for extraction. The organic phase was washed with water, dried over anhydrous sodium sulfate, and evaporated to remove the solvent to produce 2,2-diphenyl ethanol (17 g) in a yield of 92.4%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09198902B2uspto-grants-2015_12