Nitric Acid → 4-(Benzyloxy)-2-nitrophenol
Reaction equation
[C:1]1([CH2:7][O:8][C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N+:16]([O-])([OH:18])=[O:17]>C(O)(=O)C>[N+:16]([C:11]1[CH:10]=[C:9]([O:8][CH2:7][C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:14]=[CH:13][C:12]=1[OH:15])([O-:18])=[O:17]Participants
4
Reagents, catalysts & solvents 1
Procedure
4-Phenylmethoxy-phenol in acetic acid is nitrated by contact with a slight molar excess of nitric acid at room temperature, giving 2-nitro-4-phenylmethoxy-phenol.
Workup
- customat room temperature
Sources & evidence
- ORD record
- ord-4d4659e7219844c9aeaef264dcb5cafb
- Source dataset
- uspto-grants-1992_01
- Patent number
- US05082847
Reaction notes
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