Dimethylformamide → HCID 178482591, compound

HRID 437757Notes

Reaction equation

HRID 437757 reaction equation
[I-:1].Cl[C:3]1[N:4]([CH3:15])[N+:5]([CH3:14])=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:7]=1.[O-]C1C=CC=CC=1.[Na+].[CH3:24][N:25](C)[CH:26]=O>>[I-:1].[CH3:14][N+:5]1[N:4]([CH3:15])[C:3]([N:25]([CH3:26])[CH3:24])=[CH:7][C:6]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

Participants

4

Reactant 3

HCID 6228DimethylformamideHCID 4445035Phenolate SodiumHCID 12665791HCID 12665791, compound

Product 1

HCID 178482591HCID 178482591, compound

Procedure

3-Chloro-1,2-dimethyl-5-phenylpyrazolium iodide (10.0 g, 0.03 mole) is treated with sodium phenoxide (5.64 g, 0.06 mole) in dimethylformamide (100 ml) and the mixture heated and stirred at 110° C. to 120° C. for 21 hours. The dimethylformamide is then removed in vacuo, the residual oil dissolved in aqueous sodium bicarbonate solution and is extracted with ether. The ether fraction yields some brown oil which is not further examined. Next the aqueous sodium bicarbonate solution is extracted with chloroform (2× 150 ml). Evaporation of the chloroform solution yields a white solid which is dried by azeotropic distillation of toluene. Crystallization from a chloroform/ether mixture yields a white solid, m.p. 181.5° C. to 182° C.

Workup

  1. temperaturethe mixture heated
  2. customThe dimethylformamide is then removed in vacuo
  3. dissolutionthe residual oil dissolved in aqueous sodium bicarbonate solution
  4. extractionis extracted with ether
  5. customThe ether fraction yields some brown oil which
  6. extractionNext the aqueous sodium bicarbonate solution is extracted with chloroform (2× 150 ml)
  7. customEvaporation of the chloroform solution
  8. customyields a white solid which
  9. dry with materialis dried by azeotropic distillation of toluene
  10. customCrystallization from a chloroform/ether mixture
  11. customyields a white solid, m.p. 181.5° C. to 182° C.

Sources & evidence

ORD record
ord-a2f435dd66aa454bb0874f3d937b099d
Source dataset
uspto-grants-1977_06
Patent number
US04032526

Reaction notes

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