Methyl pyruvate → HCID 72321878, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][NH2:10])=[C:5]([N+:11]([O-:13])=[O:12])[CH:4]=1.[C:14]([O:19][CH3:20])(=[O:18])[C:15]([CH3:17])=O.C([O-])(=O)C.[Na+]>CO>[CH3:20][O:19][C:14](=[O:18])[C:15](=[N:10][NH:9][C:6]1[CH:7]=[CH:8][C:3]([Cl:2])=[CH:4][C:5]=1[N+:11]([O-:13])=[O:12])[CH3:17]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
(4-Chloro-2-nitro-phenyl)hydrazine hydrochloride (30 g, 0.14 mol) prepared in Step A and methyl pyruvate (14.4 mL, 0.16 mol) were dissolved in methanol (300 mL), and sodium acetate (14.2 g, 0.17 mol) was added thereto. The reaction solution was stirred for 8 h at room temperature, and the resulting yellow solid was filtered, washed with water and methanol, and dried to give the title compound (30 g, Yield 82%).
Workup
- filtrationthe resulting yellow solid was filtered
- washwashed with water and methanol
- customdried
Sources & evidence
- ORD record
- ord-b51b517fca5541fe80d243a8f7242fd6
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08889691B2
Reaction notes
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