Triethylamine → Benzyl 4,4-bis(2-hydroxyethyl)piperidine-1-carboxylate
Reaction equation
[OH:1][CH2:2][CH2:3][C:4]1([CH2:10][CH2:11][OH:12])[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1.Cl[C:14]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:15].C(N(CC)CC)C>O1CCCC1>[CH2:17]([O:16][C:14]([N:7]1[CH2:8][CH2:9][C:4]([CH2:3][CH2:2][OH:1])([CH2:10][CH2:11][OH:12])[CH2:5][CH2:6]1)=[O:15])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
5
Procedure
1-benzyloxycarbonyl-4,4-bis-(2-hydroxyethyl)piperidine is prepared by reaction of 4,4-bis-(2-hydroxyethyl)piperidine with benzyl chloroformate in tetrahydrofuran in the presence of triethylamine.
Sources & evidence
- ORD record
- ord-36b52ce730f54afaae321c23661510b3
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06627634B2
Reaction notes
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