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

HRID 1692579Notes

Reaction equation

HRID 1692579 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-196e7eb40f2045308d3b594a2b3538be
Source dataset
uspto-grants-2012_04
Patent number
US08158619B2

Reaction notes

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