Sodium hydride → HCID 19926616, compound

HRID 1647239Notes

Reaction equation

HRID 1647239 reaction equation
F[C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.[N+:10]([C:13]1[N:14]=[CH:15][NH:16][CH:17]=1)([O-:12])=[O:11].[H-].[Na+]>CN(C)C=O>[N+:10]([C:13]1[N:14]=[CH:15][N:16]([C:2]2[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=2)[CH:17]=1)([O-:12])=[O:11]

Participants

5

Reactant 3

HCID 24758Sodium hydrideHCID 680234-FluorobenzaldehydeHCID 178526856HCID 178526856, compound

Product 1

HCID 19926616HCID 19926616, compoundYield 55.3%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent2×

Procedure

A suspension of 18.6 g of 4-fluorobenzaldehyde and 18.6 g of 4-nitroimidazole in 70 ml of dimethylformamide was dropwise added to a suspension of 6.6 g of sodium hydride (60% suspension in mineral oil) in 150 ml of dimethylformamide at a room temperature under stirring. The obtained mixture was stirred at 90° C. for about 5 hours, cooled and poured into ice-water to precipitate a solid. This solid was recovered by filtration, washed with water and heated together with ethanol. The mixture was cooled and filtered. The obtained solid was washed with ethanol to obtain 18 g of the title compound as a white powder (yield: 55%).

Workup

  1. stirringThe obtained mixture was stirred at 90° C. for about 5 hours
  2. temperaturecooled
  3. customto precipitate a solid
  4. filtrationThis solid was recovered by filtration
  5. washwashed with water
  6. temperatureheated together with ethanol
  7. temperatureThe mixture was cooled
  8. filtrationfiltered
  9. washThe obtained solid was washed with ethanol

Sources & evidence

ORD record
ord-f0c1b7566124496a8adc27fc95c8016d
Source dataset
uspto-grants-1995_07
Patent number
US05430059

Reaction notes

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