Methyl (2-aminoindan-5-yl)acetate hydrochloride → 2-Aminoindane-5-acetic acid hydrochloride
Reaction equation
[ClH:1].[NH2:2][CH:3]1[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH2:12][C:13]([O:15]C)=[O:14])[CH:9]=2)[CH2:4]1>Cl>[ClH:1].[NH2:2][CH:3]1[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH2:12][C:13]([OH:15])=[O:14])[CH:9]=2)[CH2:4]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
3.6 g of methyl 2-aminoindane-5-acetatehydrochloride are refluxed for 3 hours in 160 ml of semiconcentrated hydrochloric acid. The hydrochloric acid is distilled off and the remaining product is triturated with a little ethanol, suction filtered and dried in vacuo.
Workup
- distillationThe hydrochloric acid is distilled off
- customthe remaining product is triturated with a little ethanol, suction
- filtrationfiltered
- customdried in vacuo
Sources & evidence
- ORD record
- ord-9ad09ef9d76a46ef9b8d69b40e8a8f64
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05591769
Reaction notes
Loading…