HCID 21837219, compound → 1-(3-Ethylphenyl)piperazine
Reaction equation
C([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20][CH3:21])[CH:15]=2)[CH2:10][CH2:9]1)(OC(C)(C)C)=O>CCOC(C)=O>[CH2:20]([C:16]1[CH:15]=[C:14]([N:11]2[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]2)[CH:19]=[CH:18][CH:17]=1)[CH3:21]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
0.037 g (0.128 mmol) 1-Boc-4-(3-ethylphenyl)-piperazine from the previous step was dissolved in 10 mL EtOAc and cooled to 0° C. using an ice bath. HCl gas was then bubbled through the reaction for 10 min, followed by an additional 10 min of stirring. The reaction was warmed to ambient temperature and the solvent removed in vacuo. The residue was taken up in 10 mL CHCl3 that had been previously saturated with NH3 gas, the solid NH4Cl filtered, and the solvent removed to give 1-(3-ethylphenyl)piperazine as the free base.
Workup
- customHCl gas was then bubbled through the reaction for 10 min
- temperatureThe reaction was warmed to ambient temperature
- customthe solvent removed in vacuo
- filtrationthe solid NH4Cl filtered
- customthe solvent removed
Sources & evidence
- ORD record
- ord-5dd28b3b4fa74fa1818ce9ff72830c03
- Source dataset
- uspto-grants-1999_10
- Patent number
- US05968938
Reaction notes
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