反応 #722766

ord-58a7450bdc1c4b73b3b7188f5530d838

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted with Et2O (3×40 ml)
  2. 2
    洗浄The combined organic layers were washed with water, sat. aqueous NaHCO3 and brine
  3. 3
    乾燥dried over MgSO4
  4. 4
    濃縮concentrated in vacuo
  5. 5
    その他Purification
  6. 6
    workup.DISTILLATIONby Kugelrohr distillation

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06187933B1uspto-grants-2001_02