Hydrochloric Acid → cis-3-Amino-4-methoxypyrrolidine dihydrochloride
Reaction equation
[ClH:1].[NH2:2][CH:3]1[CH:7]([O:8][CH3:9])[CH2:6][N:5](C(OC(C)(C)C)=O)[CH2:4]1>C(O)C>[ClH:1].[ClH:1].[NH2:2][C@H:3]1[C@@H:7]([O:8][CH3:9])[CH2:6][NH:5][CH2:4]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
64 ml of 6N aqueous hydrochloric acid were added to a solution of 4.16 g (0.019 mole) of 3-amino-1-t-butoxycarbonyl-4-methoxypyrrolidine in 200 ml of ethanol, and the mixture was heated under reflux for 1 hour. At the end of this time, the solvent was completely removed by evaporation to dryness under reduced pressure to obtain cis-3-amino-4-methoxypyrrolidine dihydrochloride as a brown powder. The whole of this dihydrochloride was dissolved in 20 ml of water, 1.97 g (0.037 mole) of sodium methoxide was added thereto, and the solvent was removed by evaporation under reduced pressure to give a residue, which was washed with a 1:1 by volume mixture of ethanol and ethyl acetate. The washings were concentrated by evaporation under reduced pressure to afford 2.06 g of cis-3-amino-4-methoxypyrrolidine as a brown oily substance.
Workup
- temperaturethe mixture was heated
- temperatureunder reflux for 1 hour
- customAt the end of this time, the solvent was completely removed by evaporation to dryness under reduced pressure
Sources & evidence
- ORD record
- ord-eda12e5447094ba7984f1b9608bffc8e
- Source dataset
- uspto-grants-1991_03
- Patent number
- US04997943
Reaction notes
Loading…