Styphnic acid → Dipyridinium styphnate

HRID 1413541Notes

Reaction equation

HRID 1413541 reaction equation
[C:1]1([C:16]([OH:17])=[C:12]([N+:13]([O-:15])=[O:14])[CH:11]=[C:7]([N+:8]([O-:10])=[O:9])[C:5]=1[OH:6])[N+:2]([O-:4])=[O:3]>N1C=CC=CC=1>[C:1]1([C:5]([O-:6])=[C:7]([N+:8]([O-:10])=[O:9])[CH:11]=[C:12]([N+:13]([O-:15])=[O:14])[C:16]=1[O-:17])[N+:2]([O-:4])=[O:3].[NH+:8]1[CH:7]=[CH:11][CH:12]=[CH:16][CH:1]=1.[NH+:8]1[CH:7]=[CH:11][CH:12]=[CH:16][CH:1]=1

Participants

3

Procedure

500 grams (2.04 moles) of dry styphnic acid are added in portions, with vigorous stirring, to two liters of dry pyridine. The mixture warms up slightly and a yellow reaction product precipitates. The mixture is stirred for another hour in the warm state, and then the cooled mixture is freed of solids by filtration. The solids are washed with one liter of ether, suspended in two liters of ether, freed of the solvent by filtration, again washed with 500 ml of ether, and dried in air.

Workup

  1. customa yellow reaction product precipitates
  2. filtrationthe cooled mixture is freed of solids by filtration
  3. washThe solids are washed with one liter of ether
  4. filtrationfreed of the solvent by filtration
  5. washagain washed with 500 ml of ether
  6. customdried in air

Sources & evidence

ORD record
ord-b93c525ea49c4822bac41d55275010b1
Source dataset
uspto-grants-1981_02
Patent number
US04250294

Reaction notes

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