Hydrochloric Acid → HCID 88177698, compound
Reaction equation
[ClH:1].[CH3:2][N:3]([CH3:33])[CH2:4][CH2:5][CH2:6][NH:7][C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[N:18]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH:19]=[O:20])=[O:9]>C(OCC)(=O)C>[ClH:1].[CH3:33][N:3]([CH3:2])[CH2:4][CH2:5][CH2:6][NH:7][C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[N:18]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH:19]=[O:20])=[O:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4N Hydrochloric acid--ethyl acetate solution (0.13 ml) was added to a solution of [2-[[N-[3-(dimethylamino)propyl]carbamoyloxy]methyl]phenyl]-N-dodecylformamide (0.200 g) in ethyl acetate (2 ml) at room temperature. After being stirred for 15 minutes, the reaction mixture was concentrated, thereby yielding 0.217 g of the aimed compound as white solid.
Workup
- concentrationthe reaction mixture was concentrated
Sources & evidence
- ORD record
- ord-af4efa3d179b4c3f800f6a6e5e1ed9f4
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06114325
Reaction notes
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