Benzyl 3-(2-hydroxyethyl)piperidine-1-carboxylate → Benzyl 3-(2-bromoethyl)piperidine-1-carboxylate
Reaction equation
[Br:1]CCCC1CCCCN1C(OCC1C=CC=CC=1)=O.O[CH2:22][CH2:23][CH:24]1[CH2:29][CH2:28][CH2:27][N:26]([C:30]([O:32][CH2:33][C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)=[O:31])[CH2:25]1>>[Br:1][CH2:22][CH2:23][CH:24]1[CH2:29][CH2:28][CH2:27][N:26]([C:30]([O:32][CH2:33][C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)=[O:31])[CH2:25]1Participants
3
Procedure
Prepared similarly to Intermediate 10 from phenylmethyl 3-(2-hydroxyethyl)-1-piperidinecarboxylate (for example, as prepared for Intermediate 15).
Sources & evidence
- ORD record
- ord-1ed850e3e8564846a4069bbf9b8ee4be
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08575340B2
Reaction notes
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