Hydrazine → 3-Hydroxy-4-methylbenzohydrazide
Reaction equation
C([O:3][C:4](=O)[C:5]1[CH:10]=[CH:9][C:8]([CH3:11])=[C:7]([OH:12])[CH:6]=1)C.[NH2:14][NH2:15]>>[OH:12][C:7]1[CH:6]=[C:5]([CH:10]=[CH:9][C:8]=1[CH3:11])[C:4]([NH:14][NH2:15])=[O:3]Participants
3
Conditions
- Temperature
- 150 °C
Procedure
A suspension of ethyl 3-hydroxy-4-methylbenzoate (14.42 g, 80 mmol) (from Example 32 supra) in anhydrous hydrazine (30 mL, 956 mmol) (Aldrich) was heated at reflux (150° C. bath temperature) for 2.0 hours. After cooling to room temperature, mixture was concentrated under reduced pressure (high vacuum) to give crude 3-hydroxy-4-methyl-benzoic acid hydrazide as an off-white solid. (Yield 13.26 g, 100%).
Workup
- temperaturewas heated
- temperatureAfter cooling to room temperature
- concentrationmixture was concentrated under reduced pressure (high vacuum)
Sources & evidence
- ORD record
- ord-855f72b9cbe74fd98db79a8199c8e3ca
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07994321B2
Reaction notes
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