2-Hydroxy-5-nitroindane → 5-amino-2,3-dihydro-1H-inden-2-ol

HRID 1422848Notes

Reaction equation

HRID 1422848 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]2

Participants

3

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

  1. customat room temperature
  2. filtrationPd/C was filtered off through a pad of celite
  3. concentrationthe mother liquid was concentrated

Sources & evidence

ORD record
ord-960efe60fb0a423c8648676886e9ecd2
Source dataset
uspto-grants-2015_01
Patent number
US08927548B2

Reaction notes

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