5-Nitrofurfural → HCID 178419257, compound
Reaction equation
[N+:1]([C:4]1[O:8][C:7]([CH:9]=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[BrH:11].Br.[CH3:13][N:14]([CH3:23])[CH2:15][CH2:16][CH2:17][NH:18][C:19]([NH:21][NH2:22])=[NH:20]>C(O)C>[BrH:11].[BrH:11].[N+:1]([C:4]1[O:8][C:7]([CH:9]=[N:22][NH:21][C:19](=[NH:20])[NH:18][CH2:17][CH2:16][CH2:15][N:14]([CH3:23])[CH3:13])=[CH:6][CH:5]=1)([O-:3])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5-Nitro-2-furaldehyde (0.564 g, 4 mmole) and N-(3-dimethylaminopropyl)hydrazinecarboximidamide dihydrobromide (1.6 g, 5 mmole) are heated at reflux in 8 ml 95% ethanol for 1 hour. The title compound precipitates from solution on cooling and is recrystallized from ethanol, mp 131°-133° C.
Workup
- customThe title compound precipitates from solution
- temperatureon cooling
- customis recrystallized from ethanol, mp 131°-133° C.
Sources & evidence
- ORD record
- ord-1e2c22b5f5314eba8bd3b446c2fc4025
- Source dataset
- uspto-grants-1992_09
- Patent number
- US05145975
Reaction notes
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