1,4-Dioxane → 1,4-Diazabicyclo(3.2.2)nonane

HRID 1157133Notes

Reaction equation

HRID 1157133 reaction equation
[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[NH:4][C:3](=O)[CH2:2]2.O1CCOCC1>O>[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[NH:4][CH2:3][CH2:2]2

Participants

4

Procedure

To the solution of 1,4-diazabicyclo[3.2.2]nonan-3-one (15.8 g; 113 mmol) in absolute dioxane (130 ml) LiAlH4 (4.9 g; 130 mmol) was added under argon. The mixture was refluxed for 6 hours and then allowed to reach room temperature. To the reaction mixture water (5 ml in 10 ml of dioxane) was added by drops, the mixture was stirred for 0.5 hour and then filtered off via glass filter. The solvent was evaporated and the residue was distilled using Kugelrohr apparatus at 90° C. (0.1 mbar) to yield 1,4-diazabicyclo[3.2.2]nonane (11.1 g; 78%) as colourless hygroscopic material.

Workup

  1. temperatureThe mixture was refluxed for 6 hours
  2. customto reach room temperature
  3. filtrationfiltered off via glass
  4. filtrationfilter
  5. customThe solvent was evaporated
  6. distillationthe residue was distilled
  7. customat 90° C.

Sources & evidence

ORD record
ord-bce0685ecac1462e8853a20c3b2c75ff
Source dataset
uspto-grants-2010_10
Patent number
US07807667B2

Reaction notes

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