Oxalic Acid → HCID 178526554, compound
Reaction equation
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[C:12](O)(=[O:16])[C:13](O)=[O:14]>C(O)(=O)C>[OH:14][C:13]1[C:12]([OH:16])=[N:1][C:2]2[C:7](=[CH:6][CH:5]=[CH:4][C:3]=2[N+:9]([O-:11])=[O:10])[N:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4 g (26.12 mmol) of 2,3-diaminonitrobenzene and 6.59 g (52.24 mmol) of commercial oxalic acid were dissolved in 50% acetic acid, and reaction was allowed at boiling point under an argon stream for 3 hr. After the reaction was over, the reaction mixture was cooled to room temperature, and the crystal precipitated was filtered out.
Workup
- customreaction
- customfor 3 hr
- customthe crystal precipitated
- filtrationwas filtered out
Sources & evidence
- ORD record
- ord-957c8cffcf9a4f65b3534c2f012d8a63
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06822069B2
Reaction notes
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