Hydrochloric Acid → HCID 68110022, compound
Reaction equation
[CH3:1][N:2]([CH3:20])[CH:3]1[CH2:8][CH2:7][CH:6]([N:9]([CH2:17][CH2:18][OH:19])C(=O)OC(C)(C)C)[CH2:5][CH2:4]1.[ClH:21]>ClCCl>[ClH:21].[CH3:1][N:2]([CH3:20])[CH:3]1[CH2:4][CH2:5][CH:6]([NH:9][CH2:17][CH2:18][OH:19])[CH2:7][CH2:8]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 5 °C
Procedure
To a 100-mL round-bottom flask was added a solution of tert-butyl N-[4-(dimethylamino)cyclohexyl]-N-(2-hydroxyethyl)carbamate (3.0 g, 10.47 mmol, 1.00 equiv) in dichloromethane (50 mL). To this solution was added hydrogen chloride (gas). The resulting solution was stirred for 3 h at 0-10° C. The resulting mixture was concentrated under vacuum to give 2.0 g (86%) of 2-[[4-(dimethylamino)cyclohexyl]amino]ethan-1-ol hydrochloride as a yellow oil. MS: m/z 187 (M+H)+.
Workup
- concentrationThe resulting mixture was concentrated under vacuum
Sources & evidence
- ORD record
- ord-d3b4533d3e07427689c2ec2600ef1dd0
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09340554B2
Reaction notes
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