Hydrochloric Acid → HCID 68706690, compound
Reaction equation
C(OC(=O)[NH:7][CH2:8][C:9]1([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:14][CH2:13][N:12]([C:15](=[O:17])[CH3:16])[CH2:11][CH2:10]1)(C)(C)C.[ClH:25]>CCOCC.O1CCOCC1>[ClH:25].[NH2:7][CH2:8][C:9]1([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:10][CH2:11][N:12]([C:15](=[O:17])[CH3:16])[CH2:13][CH2:14]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of (1-acetyl-4-phenylpiperidin-4-ylmethyl)carbamic acid tert-butyl ester in ether is added 4 N HCl in 1,4-dioxane. The reaction mixture is stirred at room temperature for 1 h, and concentrated in vacuo. The resulting solid is washed with ether to give the title compound, which is directly used for the next reaction without further purification.
Workup
- concentrationconcentrated in vacuo
- washThe resulting solid is washed with ether
Sources & evidence
- ORD record
- ord-eb968db4ea084ac79dd1ef5970d10c29
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07704996B2
Reaction notes
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