Acetone → N'-(propan-2-ylidene)isonicotinohydrazide
Reaction equation
[C:1]([NH:9][NH2:10])(=[O:8])[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.[CH3:11][C:12]([CH3:14])=O>>[CH3:11][C:12](=[N:10][NH:9][C:1](=[O:8])[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1)[CH3:14]Participants
3
Conditions
- Temperature
- 20 °C
Procedure
A four neck flask (1 liter) equipped with a thermometer, a reflux condenser and a stirrer was charged with 68.5 g (0.5 mol) of isonicotinohydrazide and 500 ml of acetone and then heated under reflux for 24 hours. The reaction liquid was cooled down to 20° C. or lower, and then crystal was filtered off and dried under reduced pressure, whereby the intended compound (white crystal) was obtained.
Workup
- customA four neck flask (1 liter) equipped with a thermometer, a reflux condenser and a stirrer
- temperatureheated
- temperatureunder reflux for 24 hours
- customThe reaction liquid
- filtrationlower, and then crystal was filtered off
- customdried under reduced pressure, whereby the intended compound (white crystal)
- customwas obtained
Sources & evidence
- ORD record
- ord-c3f313a0529d4c6bbcb1afb3ba6737ff
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06380288B1
Reaction notes
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