Réaction #2195474

ord-af90bdee04c6435ab7f16f67a8b833d8

Équation de réaction

CC(C)[N-]C(C)C.[Li+]
lithium diisopropylamide
C1CCCCC1.C1CCOC1.CCc1ccccc1
cyclo-hexane ethylbenzene THF
Cl
hydrochloric acid
OC(c1ccccc1)c1ccccc1
diphenyl-methanol
Rendement 83.0%
OC(c1ccccc1)c1ccccc1
diphenylmethanol
Rendement 83.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONare added to the batch
  2. 2
    ExtractionThe aqueous phase is extracted with MTB ether
  3. 3
    Lavagethe organic phase is washed with sat. sodium chloride solution
  4. 4
    Séchagedried over sodium sulfate
  5. 5
    Autreevaporated

Mode opératoire

16.1 ml (120 mmol) of a 2M solution of lithium diisopropylamide in cyclo-hexane/ethylbenzene/THF are added under nitrogen and at −70° C. to a solution of 24.0 g (110 mmol) of the aromatic compound 24 in 150 ml of THF. After 1.5 hours at the low temperature, 22.1 g (100 mmol) of the aldehyde 23, dissolved in 50 ml of THF, are added to the batch. After 3 hours at −70° C., the batch is warmed to room temperature, hydrolysed and acidified using hydrochloric acid. The aqueous phase is extracted with MTB ether, and the organic phase is washed with sat. sodium chloride solution, dried over sodium sulfate, evaporated and passed through silica gel (MTB ether/n-heptane 1:10), giving 40.2 g (83%) of the diphenyl-methanol 25.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07514127B2uspto-grants-2009_04