Formic Acid → HCID 178517978, compound
Reaction equation
[C:1]1([NH:7][NH:8][C:9]([NH2:11])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:12](O)=O.S(=O)(=O)(O)O>O>[C:1]1([N:7]2[CH:12]=[N:11][C:9]([OH:10])=[N:8]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
151 g of 1-phenyl semicarbazide, 135.3 g (2.5 mols) of 85% formic acid (technical) and 25 g (0.25 mol) of concentrated sulfuric acid were stirred for six hours at 95° to 100° C. The viscous mass obtained was diluted with 400 ml of water and cooled. The precipitate consisting of 1-phenyl-1,2,4-triazolone-3 was filtered off and washed neutral with water. Drying at 100° C. and 200 mbar gave 145.5 g=90.3% of the theory, of 1-phenyl-1,2,4-triazolone-3 having a melting point of 285° to 286° C. ##STR2##
Workup
- customThe viscous mass obtained
- temperaturecooled
- filtrationwas filtered off
- washwashed neutral with water
- customDrying at 100° C.
- custom200 mbar gave 145.5 g=90.3% of the theory
Sources & evidence
- ORD record
- ord-3c3c237d012e4669b0c27ad0f2f8d64f
- Source dataset
- uspto-grants-1984_08
- Patent number
- US04467098
Reaction notes
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