反応 #543543

ord-f13c8d6f5eec4384a33b4efb236d4d6e

反応方程式

C1CCNC1
pyrrolidine
c1ccncc1
pyridine
O=C(Cl)C12CC3CC(C(=O)Cl)(C1)CC(C(=O)Cl)(C3)C2
1,3,5-adamantanetricarbonyl trichloride
O=C(N1CCCC1)C12CC3CC(C(=O)N4CCCC4)(C1)CC(C(=O)N1CCCC1)(C3)C2
1,3,5-tris(1-pyrrolidinylcarbonyl)adamantane
収率 90.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他In a 500-ml flask equipped with a stirrer
  2. 2
    workup.ADDITIONwas added dropwise over 1 hour
  3. 3
    洗浄was washed with water, 1 N hydrochloric acid, and 10% aqueous sodium carbonate solution
  4. 4
    その他the solvent was removed under reduced pressure

実験手順

In a 500-ml flask equipped with a stirrer, a thermometer and a dropping funnel were placed 34.5 g (485 mmol) of pyrrolidine, 38.4 g (485 mmol) of pyridine and 140 ml of methylene chloride. To the stirred mixture under ice-cooling in a nitrogen atmosphere, 31.4 g (97 mmol) of 1,3,5-adamantanetricarbonyl trichloride in 190 ml of methylene chloride was added dropwise over 1 hour. This was warmed to room temperature, was stirred for further 1 hour and was washed with water, 1 N hydrochloric acid, and 10% aqueous sodium carbonate solution, and the solvent was removed under reduced pressure, to yield 37.2 g (87 mmol) of 1,3,5-tris(1-pyrrolidinylcarbonyl)adamantane in a yield of 90%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07186454B2uspto-grants-2007_03