2-Nitroresorcinol → 2-Aminoresorcinol
Reaction equation
[N+:1]([C:4]1[C:10]([OH:11])=[CH:9][CH:8]=[CH:7][C:5]=1[OH:6])([O-])=O>C(O)C.ClCCl.[Pt](=O)=O>[NH2:1][C:4]1[C:10]([OH:11])=[CH:9][CH:8]=[CH:7][C:5]=1[OH:6]Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
A suspension of 2-nitroresorcinol (4.995 g) and platinum (IV) oxide (356 mg) in ethanol (90 ml) was hydrogenated, at room temperature, at 100 p.s.i. for 4 hours. The reaction mixture was filtered through celite, the filter cake washed with methanol (50 ml), and the combined filtrate evaporated in-vacuo to yield a brown solid. The solid was suspended in dichloromethane (100 ml) and evaporated to dryness to yield the title compound (3.83 g, 95%) as a brown solid.
Workup
- customwas hydrogenated, at room temperature, at 100 p.s.i
- filtrationThe reaction mixture was filtered through celite
- washthe filter cake washed with methanol (50 ml)
- customthe combined filtrate evaporated in-vacuo
- customto yield a brown solid
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-75a64971048643eb81e1d6b81fa57a58
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06372770B1
Reaction notes
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