2-Hydroxy-5-nitroindane → 5-amino-2,3-dihydro-1H-inden-2-ol
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([OH:13])[CH2:7]2)([O-])=O>[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([OH:13])[CH2:7]2Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
5-nitro-indan-2-ol (450 mg, 2.5 mmol) was hydrogenated using Pd/C (10%, dry, 100 mg) and H2 balloon at 1 atm at room temperature. Pd/C was filtered off through a pad of celite and the mother liquid was concentrated to give the crude product, 5-Amino-indan-2-ol.
Workup
- customat room temperature
- filtrationPd/C was filtered off through a pad of celite
- concentrationthe mother liquid was concentrated
Sources & evidence
- ORD record
- ord-c1e9be6881714f089dafe369bae5c784
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318790B2
Reaction notes
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