Formaldehyde → 1H-Pyrrole-2-methanamine, N,N,1-trimethyl-

HRID 562633Notes

Reaction equation

HRID 562633 reaction equation
[CH2:1]=O.Cl.[CH3:4][NH:5][CH3:6].[CH3:7][N:8]1[CH:12]=[CH:11][CH:10]=[CH:9]1>[OH-].[Na+]>[CH3:4][N:5]([CH2:1][C:9]1[N:8]([CH3:7])[CH:12]=[CH:11][CH:10]=1)[CH3:6]

Participants

5

Procedure

A mixture of 35% aqueous formaldehyde solution (20.8 ml, 264.3 mmol) and dimethylamine hydrochloride (22.70 g, 278.4 mmol) was added to 1-methylpyrrole (21.42 g, 264.1 mmol) with stirring under ice-cooling over a 90-minute interval, and then the resulting mixture was stirred at room temperature for 6 hours. After stirring, 10% aqueous sodium hydroxide solution (150 ml) was added to the reaction mixture, and the reaction mixture was extracted with ether. The extract was washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. After filtration, the solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of dichloromethane and methanol (10:1) as the eluent to afford 2-(N,N-dimethylaminomethyl)-1-methylpyrrole (31.47 g, yield: 86%).

Workup

  1. temperaturecooling over a 90-minute interval
  2. stirringthe resulting mixture was stirred at room temperature for 6 hours
  3. stirringAfter stirring
  4. extractionthe reaction mixture was extracted with ether
  5. washThe extract was washed with saturated aqueous sodium chloride solution
  6. dry with materialdried over anhydrous sodium sulfate
  7. filtrationAfter filtration
  8. customthe solvent was removed in vacuo
  9. customthe residue was purified by chromatography on a silica gel column

Sources & evidence

ORD record
ord-d693ac37f1934e2fa22458360670ddd5
Source dataset
uspto-grants-2011_11
Patent number
US08067396B2

Reaction notes

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