Hydrazine hydrate (1:1) → 4-Isobutylbenzohydrazide
Reaction equation
O.[NH2:2][NH2:3].[CH2:4]([C:8]1[CH:18]=[CH:17][C:11]([C:12](OCC)=[O:13])=[CH:10][CH:9]=1)[CH:5]([CH3:7])[CH3:6]>O>[CH2:4]([C:8]1[CH:18]=[CH:17][C:11]([C:12]([NH:2][NH2:3])=[O:13])=[CH:10][CH:9]=1)[CH:5]([CH3:7])[CH3:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrazine monohydrate (2.43 g, 48.5 mmol) was added slowly to a heterogeneous solution of ethyl 4-isobutylbenzoate (5.0 g, 24.2 mmol) and H2O and stirred at reflux for 12 hours. The reaction mixture was cooled to room temperature and filtered. The yellow solid was washed with cold water (1×20 mL) and dried to provide the title compound (3.33 g, 78% yield) as a yellow solid.
Workup
- temperatureat reflux for 12 hours
- filtrationfiltered
- washThe yellow solid was washed with cold water (1×20 mL)
- customdried
Sources & evidence
- ORD record
- ord-24d2ab6c494d486e82e639d6eeae7889
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07671043B2
Reaction notes
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