Hydrochloric Acid → 1-Aminoindane Hydrochloride
Reaction equation
C([NH:8][CH:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:11][CH2:10]1)(OC(C)(C)C)=O.[ClH:18]>O1CCOCC1>[ClH:18].[NH2:8][CH:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:11][CH2:10]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6-(N-Me, N-Et Carbamyloxy) N-Boc aminoindan (7.8 g. 23.3 mmol) was dissolved in dioxane (80 ml), and a 20% solution of gas. HCl in dioxane (80 ml) was added. After 2 hr stirring at RT the solvent was evaporated in-vacuo and the residue was treated with dry ether (200 ml) and the mixture stirred at RT for 4 hrs and filtered, to give 6.15 g (0.7 mmol, 97%) of 6-(N-Me, N-Et carbamyloxy) aminoindan hydrochloride.
Workup
- customwas evaporated in-vacuo
- additionthe residue was treated with dry ether (200 ml)
- stirringthe mixture stirred at RT for 4 hrs
- filtrationfiltered
Sources & evidence
- ORD record
- ord-b93b5d5f3b5c4e7abe73a424346e6d13
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06462222B1
Reaction notes
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