Reaction #741715

ord-d80d8268f58f4eb0bcad855845c0352c

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherAfter the reaction
  2. 2
    Otherthe solvent was evaporated in vacuo and ether-water
  3. 3
    workup.ADDITIONwas added to the residue
  4. 4
    Extractionto extract unreacted reactants in the etherial layer
  5. 5
    Filtrationfiltered
  6. 6
    Washwashed
  7. 7
    Otherdried

Procedure

4.218 g (0.03 mol) of α-methylbenzyl chloride and 3.638 g (0.03 mol) of N,N-dimethylaniline were reacted in 40 ml of methanol at 40° C. for 3 days. After the reaction, the solvent was evaporated in vacuo and ether-water was added to the residue to extract unreacted reactants in the etherial layer. To the aqueous layer was added 7.77 g (0.03 mol) of sodium hexafluoroantimonate. The resulting crystals were suction filtered, washed and dried to give the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05132377uspto-grants-1992_07