反応 #52302

ord-b1d78607255e4db591db91c514e39db9

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    その他the ice-water bath was removed
  3. 3
    その他quenched with saturated NaHCO3
  4. 4
    その他Aqueous was separated
  5. 5
    抽出extracted with dichloromethane (2 times)
  6. 6
    乾燥dried over Na2SO4
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    ろ過filtered
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    濃縮concentrated
  9. 9
    その他to give a redish colored residue, that
  10. 10
    ろ過was filtered through a short path silica gel plug
  11. 11
    洗浄eluting with DCM/hexane (10% to 20%)

実験手順

To a solution of piperonal (4.5 g, 30 mmol) and triphenylphosphine (24 g, 90 mmol) in DCM (120 mL) in an ice-water bath was added a solution of carbontetrabromide (15 g, 45 mmol) over a 10 minutes period. After the addition completed, the ice-water bath was removed, the reaction stirred at ambient temperature for 2 h, and then quenched with saturated NaHCO3. Aqueous was separated, and extracted with dichloromethane (2 times). The organic layers were combined, dried over Na2SO4, filtered, and concentrated to give a redish colored residue, that was filtered through a short path silica gel plug, eluting with DCM/hexane (10% to 20%). Concentration of the filtrate gave the title compound (6.5 g, 74% yield) as a pale yellow liquid. 1H NMR (CDCl3) δ 7.36 (s, 1H), 7.18 (d, 1H, J=1.6 Hz), 6.95 (dd, 1H, J=1.5, 8.1 Hz), 6.79 (d, 1H, J=8.1 Hz), 5.99 (s, 2H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06855722B2uspto-grants-2005_02