Hydrochloric Acid → HCID 70239492, compound
Reaction equation
[CH3:1][C:2]1[CH:16]=[CH:15][CH:14]=[C:13]([CH3:17])[C:3]=1[O:4][CH2:5][C@H:6]1[CH2:11][CH2:10][CH2:9][N:8]([CH3:12])[CH2:7]1.[ClH:18]>CCOCC>[ClH:18].[CH3:1][C:2]1[CH:16]=[CH:15][CH:14]=[C:13]([CH3:17])[C:3]=1[O:4][CH2:5][C@H:6]1[CH2:11][CH2:10][CH2:9][N:8]([CH3:12])[CH2:7]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The (S)-3-(2,6-dimethylphenoxymethyl)-1-methylpiperidine (8.0 g) was dissolved in ether (500 mL) and treated with a 1M solution of hydrochloric acid in ether (37.7 mL). The thick white precipitate was isolated by filtration, washed with ether (75 mL), and dried to give (S)-3-(2,6-dimethylphenoxymethyl)-1-methylpiperidine hydrochloride (8.6 g, 93%), m.p. 149.8-151.3° C.
Workup
- customThe thick white precipitate was isolated by filtration
- washwashed with ether (75 mL)
- customdried
Sources & evidence
- ORD record
- ord-66a2e9f084774f1faf7ee3897b67b7e3
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110937
Reaction notes
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