反応 #60495

ord-b057f1d877504aee9890540925269c05

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮the organic layer was concentrated
  2. 2
    その他The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane)

実験手順

To a solution of 1-[4-methoxy-2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine (10 mg, 0.030 mmol) produced in Example (85c) in tetrahydrofuran (1 mL) were added butyraldehyde (3.3 mg, 0.045 mmol), sodium triacetoxyborohydride (13 mg, 0.061 mmol) and acetic acid (1.8 mg, 0.030 mmol) in that order, followed by stirring for 60 minutes at room temperature. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture, extraction was performed with ethyl acetate, and the organic layer was concentrated. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 1-butyl-4-[4-methoxy-2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07425554B2uspto-grants-2008_09