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

HRID 1269410Notes

Reaction equation

HRID 1269410 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-8e54efb15f8a428ea6542cc179ac5d9c
Source dataset
uspto-grants-2007_04
Patent number
US07199150B2

Reaction notes

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