Water → HCID 68839036, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([C:15]([F:18])([F:17])[F:16])[CH:12]=[CH:11][C:10]=1[N+:19]([O-])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O>CC(O)=O.CCO.[Fe]>[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([C:15]([F:16])([F:17])[F:18])[CH:12]=[CH:11][C:10]=1[NH2:19])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 2-benzyloxy-1-nitro-4-trifluoromethylbenzene (1.0 g. 3.4 mmol) in 16 mL HOAc/EtOH (1:3) is added iron powder and the mixture is refluxed for 2 h. The mixture is cooled to RT and water is added and it is extracted with EtOAc. The organic phase is dried over sodium sulfate and the solvent removed under reduced pressure to give the title compound as a reddish oil.
Workup
- temperaturethe mixture is refluxed for 2 h
- extractionit is extracted with EtOAc
- dry with materialThe organic phase is dried over sodium sulfate
- customthe solvent removed under reduced pressure
Sources & evidence
- ORD record
- ord-9df361a609464c65961546419f36ac73
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084448B2
Reaction notes
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