Hydrochloric Acid → HCID 66703935, compound
Reaction equation
[ClH:1].[N:2]1([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([C@@H:17]3[O:22][CH2:21][CH2:20][N:19](C(OC(C)(C)C)=O)[CH2:18]3)=[CH:13][CH:12]=2)[CH2:6][CH2:5][CH2:4][CH2:3]1>C(OCC)(=O)C.CO>[ClH:1].[N:2]1([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:12]=[CH:13][C:14]([C@@H:17]3[O:22][CH2:21][CH2:20][NH:19][CH2:18]3)=[CH:15][CH:16]=2)[CH2:6][CH2:5][CH2:4][CH2:3]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Hydrogen chloride in ethyl acetate solution (4N) was added to a solution of tert-butyl (2S)-2-(4-(3-(pyrrolidin-1-yl)propyloxy)phenyl)morpholine-4-carboxylate (1.13 g, 2.89 mmol) in methanol. The mixture was stirred for one hour at room temperature and the solvent was evaporated under reduced pressure to give a white solid, which was recrystallized from ethanol to afford (2S)-2-(4-(3-(pyrrolidin-1-yl)propyloxy)phenyl)morpholine hydrochloride (0.9 g, 86%) as white crystals.
Workup
- customthe solvent was evaporated under reduced pressure
- customto give a white solid, which
- customwas recrystallized from ethanol
Sources & evidence
- ORD record
- ord-ebea68de88de442583e0338977c797cd
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08106045B2
Reaction notes
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