Hydrochloric Acid → 730980-52-6
Reaction equation
[ClH:1].[CH3:2][C@H:3]1[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C@@H:4]1[NH:12]C(=O)COC>C(O)C.O>[ClH:1].[NH2:12][C@H:4]1[C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH2:11][C@@H:3]1[CH3:2]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Concentrated hydrochloric acid (8 ml) was added to a solution of N-[(1R,2S)-2-methyl-1-indanyl]-2-methoxyacetamide (5.9 g, 0.0269 mol) in ethanol and water, and the mixture heated for 12 hours at reflux. The solvent was evaporated and a small amount of ethyl acetate added. The undissolved solid was filtered off to give (1R,2S)-1-amino-2-methylindane hydrochloride (1.0 g) as a solid, chemical purity>95%.
Workup
- temperaturethe mixture heated for 12 hours
- temperatureat reflux
- customThe solvent was evaporated
- additiona small amount of ethyl acetate added
- filtrationThe undissolved solid was filtered off
Sources & evidence
- ORD record
- ord-a361b52d3240489d809eb2c9b5bb01f2
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08114991B2
Reaction notes
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