Hydrochloric Acid → HCID 66905855, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:14]=[CH:15][CH:16]=1)[CH:7]=[C:8]([CH2:12][CH3:13])[C:9]([OH:11])=[O:10])([O-:3])=[O:2].Cl.[CH3:18][CH2:19]O>>[CH2:18]([O:10][C:9](=[O:11])[C:8](=[CH:7][C:6]1[CH:14]=[CH:15][CH:16]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1)[CH2:12][CH3:13])[CH3:19]Participants
4
Procedure
2-(3-Nitro-benzylidene)-butyric acid (500 mg, 2.27 mmol) was esterified by dissolving in EtOH (12.5 ml), adding conc HCl (0.25 ml) and heating to reflux for 8 h. The solvents were evaporated in vacuo to give the title compound.
Workup
- temperatureheating
- temperatureto reflux for 8 h
- customThe solvents were evaporated in vacuo
Sources & evidence
- ORD record
- ord-817c179eddcc4322bd65e6567d67fd97
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662839B2
Reaction notes
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