Hydrochloric Acid → 3-Methoxy-4-phenylaminopyrrolidine hydrochloride
Reaction equation
C(OC([N:8]1[CH2:12][CH:11]([NH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:10]([O:20][CH3:21])[CH2:9]1)=O)(C)(C)C.[ClH:22]>CO>[ClH:22].[CH3:21][O:20][CH:10]1[CH:11]([NH:13][C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:12][NH:8][CH2:9]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In 100 ml of methanol was dissolved 1.98 g (0.0068 mole) of 1-t-butoxycarbonyl-3-methoxy-4-phenylaminopyrrolidine obtained as described above, and 23.5 ml of 6N hydrochloric acid was added thereto. The mixture was left to stand at room temperature overnight. The solvent was removed under reduced pressure, and the residue was washed with ethanol to obtain 1.71 g of 3-methoxy-4-phenylaminopyrrolidine hydrochloride as white powder.
Workup
- customobtained
- additionwas added
- waitThe mixture was left
- customThe solvent was removed under reduced pressure
- washthe residue was washed with ethanol
Sources & evidence
- ORD record
- ord-0cc71dc497264b3cb7f2d3b3eb386623
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05688791
Reaction notes
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