反応 #52405

ord-9e01a64247cb4cbd93719c5bfbb13e61

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was refluxed for 3 h
  2. 2
    workup.ADDITIONpoured into ice-cold saturated aqueous sodium bicarbonate solution
  3. 3
    抽出extracted with diethyl ether (×2)
  4. 4
    乾燥The combined organic phase was dried over anhydrous sodium sulfate
  5. 5
    ろ過filtered
  6. 6
    その他evaporated in vacuo to a residue which

実験手順

A solution of 6-bromo-4,4-dimethyl-1,2,3,4-tetrahydroquinoline, available in accordance with U.S. Pat. No. 5,089,509, the specification of which is incorporated herein by reference (1.8 g, 7.5 mmol) in 10 mL of formic acid was refluxed for 3 h. The reaction mixture was then cooled to ambient temperature and poured into ice-cold saturated aqueous sodium bicarbonate solution and extracted with diethyl ether (×2). The combined organic phase was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to a residue which was subjected to flash column chromatography over silica gel (230-400 mesh) using 15-25% ethyl acetate in hexane as the eluent to afford the title compound as a pale yellow solid (1.8 g, 90%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06855512B2uspto-grants-2005_02