Hydrochloric Acid → (S)-4-(2-Amino-propan-1-yl)-morpholine
Reaction equation
C(OC(=O)[NH:7][CH:8]([CH3:16])[CH2:9][N:10]1[CH2:15][CH2:14][O:13][CH2:12][CH2:11]1)(C)(C)C.Cl>CO>[CH3:16][C@H:8]([NH2:7])[CH2:9][N:10]1[CH2:15][CH2:14][O:13][CH2:12][CH2:11]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (1-methyl-2-morpholin-4-yl-ethyl)-carbamic acid tert-butyl ester (0.30 g, 1.22 mmol) in methanol (10 mL) was added 2N HCl (5 mL) at 0° C. The reaction mixture was allowed to warm to room temperature and was stirred overnight. The solvent was removed under vacuum to give (S)-1-Methyl-2-morpholin-4-yl-ethylamine as a light yellow solid (250 mg, 96%). MS (M+H)=145.
Workup
- customThe solvent was removed under vacuum
Sources & evidence
- ORD record
- ord-405e067d86384ba488050c57309584c7
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08440708B2
Reaction notes
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