Reaction #52844

ord-121fda83a02d475a9abaa17eaf5c6112

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Extractionextracted with Et2O (3×40 ml)
  2. 2
    WashThe combined organic layers were washed with water, sat. aqueous NaHCO3 and brine
  3. 3
    Dryingdried over MgSO4
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    OtherPurification
  6. 6
    workup.DISTILLATIONby Kugelrohr distillation

Procedure

15.0 g (58.3 mmol) of 5-(3-bromophenyl)-2-methylpentan-2-ol (Compound E) was cooled to 0° C. and then 2.8 ml of conc. H2SO4 was added. The mixture was stirred for 2.5 hours, diluted with water (20 ml) and extracted with Et2O (3×40 ml). The combined organic layers were washed with water, sat. aqueous NaHCO3 and brine, dried over MgSO4 and concentrated in vacuo. Purification by Kugelrohr distillation gave the title compound as a colorless oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06855832B2uspto-grants-2005_02