反応 #73565

ord-b9ce09284a524db79767304a496b85c5

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他equipped with a mechanical stirrer under an inert atmosphere
  2. 2
    抽出The aqueous solution was extracted with chloroform (4×12.0 L)
  3. 3
    乾燥the combined organic layers were dried over anhydrous sodium sulfate (1.72 kg)
  4. 4
    ろ過The combined organic layers were filtered
  5. 5
    濃縮the filtrate was concentrated

実験手順

(2S,3R)-3-Amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane di-p-toluoyl-D-tartrate salt (3.64 kg, 5.96 mol) and 10% aqueous sodium chloride solution (14.4 L, 46.4 mol) were added to a 72 L glass reaction flask equipped with a mechanical stirrer under an inert atmosphere. 5 M Sodium hydroxide (5.09 L) was added to the stirring mixture to adjust the pH of the mixture to pH 14. The mixture was then stirred for a minimum of 10 min. The aqueous solution was extracted with chloroform (4×12.0 L), and the combined organic layers were dried over anhydrous sodium sulfate (1.72 kg). The combined organic layers were filtered, and the filtrate was concentrated to obtain (2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane (1.27 kg) as an oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08541446B2uspto-grants-2013_09