Ethyl orthoformate → HCID 178518009, compound

HRID 544741Notes

Reaction equation

HRID 544741 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH:7][NH:8][C:9]([NH2:11])=[O:10].[CH2:12](OC(OCC)OCC)C>C(O)C>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[N:7]1[CH:12]=[N:11][C:9]([OH:10])=[N:8]1

Participants

4

Reactant 2

HCID 31214Ethyl orthoformateHCID 1336606580714-38-1

Product 1

HCID 178518009HCID 178518009, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 31.9 g (0.21 m) of 2-pyridinyl- hydrazinecarboxamide and 17.50 ml of triethylorthoformate was refluxed for 6 hours with the ethanol formed as a by-product being continuously removed by distillation thereby maintaining the reaction temperature at 130°-140° C. At the completion of the reaction, the reaction mixture was coled to 15° C. and the solid 1-(2-pyridinyl)-1H-1,2,4- -triazol-3ol product was recovered by filtration. The product after washing with methylene chloride was recovered in a yield of 25.2 g (74 percent of theoretical). The product melted at 260°-262° C. and upon analysis was found to have carbon, hydrogen and nitrogen contents of 52.26, 3.90 and 34.79 percent, respectively, as compared with the theoretical contents of 51.89, 3.73 and 34.55 percent, respectively, calculated for the above named compound.

Workup

  1. customformed as a by-product being
  2. customcontinuously removed by distillation
  3. temperaturethereby maintaining the reaction temperature at 130°-140° C
  4. customAt the completion of the reaction
  5. customwas coled to 15° C.
  6. filtrationthe solid 1-(2-pyridinyl)-1H-1,2,4- -triazol-3ol product was recovered by filtration
  7. washThe product after washing with methylene chloride
  8. customwas recovered in a yield of 25.2 g (74 percent of theoretical)

Sources & evidence

ORD record
ord-a2a063a0a77a40eb88e3e58978508740
Source dataset
uspto-grants-1984_05
Patent number
US04451653

Reaction notes

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