Acetic Acid → HCID 18770447, compound

HRID 1279436Notes

Reaction equation

HRID 1279436 reaction equation
[CH2:1]([N:8]1[CH2:13][CH2:12][C:11](=O)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:15]([BH3-])#[N:16].[Na+].[CH3:19][NH:20][CH2:21][CH2:22][NH:23][CH3:24].[C:25](O)(=O)[CH3:26].C(=O)([O-])[O-].[K+].[K+].C(=O)([O-])O.[Na+]>CO>[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([N:20]([CH3:19])[CH2:21][CH2:22][N:23]([CH:11]2[CH2:12][CH2:13][N:16]([CH2:15][C:26]3[CH:25]=[CH:4][CH:3]=[CH:2][CH:1]=3)[CH2:9][CH2:10]2)[CH3:24])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

8

Procedure

After 1-benzyl-4-piperidone (5.00 g; 26 mmol) and sodium cyanoborohydride (1.25 g; 20 mmol) were added to a solution of N,N′-dimethylethylenediamine (785 mg; 8.9 mmol) in methanol (20 ml) under ice cooling. The ice bath was removed, and acetic acid (2.5 ml; 44 mmol) was added to the solution, and the mixture was stirred for 15 minutes. Potassium carbonate (3 g; 22 mmol) and a saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture to conduct extraction with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 955 mg (yield: 25%) of N,N′-bis(1-benzyl-4-piperidinyl)-N,N′-dimethylethylenediamine as a colorless oil.

Workup

  1. customThe ice bath was removed
  2. extractionextraction with chloroform
  3. washThe organic layer was washed with saturated brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe resultant crude oil was purified by column chromatography on silica gel

Sources & evidence

ORD record
ord-d13ce4fc31674676be2bb2370bf8fc87
Source dataset
uspto-grants-2002_09
Patent number
US06448242B1

Reaction notes

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