Methanol → HCID 69617874, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([C:10]2[O:11][CH:12]=[CH:13][C:14]=2[C:15]([OH:17])=[O:16])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[CH3:18]O>S(=O)(=O)(O)O>[CH3:18][O:16][C:15]([C:14]1[CH:13]=[CH:12][O:11][C:10]=1[C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1)=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-(3-nitrophenyl)furan-3-carboxylic acid (1.2 g) in methanol (200 mL) containing concentrated sulfuric acid (5 drops) was heated under reflux for 18 h. The reaction solution was evaporated to dryness under reduced pressure to give the title compound as a yellow solid (0.66 g). m.p.=93–94° C.
Workup
- temperaturewas heated
- temperatureunder reflux for 18 h
- customThe reaction solution was evaporated to dryness under reduced pressure
Sources & evidence
- ORD record
- ord-c3ca52953dba4feeb685aacafecc5dea
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07034053B2
Reaction notes
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