2-(Pyrrolidin-1-yl)carbonyl-3-hydroxy piperidine → 2-(Pyrrolidin-1-yl)methyl-3-hydroxy piperidine
Reaction equation
[N:1]1([C:6]([CH:8]2[CH:13]([OH:14])[CH2:12][CH2:11][CH2:10][NH:9]2)=O)[CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[N:1]1([CH2:6][CH:8]2[CH:13]([OH:14])[CH2:12][CH2:11][CH2:10][NH:9]2)[CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By reducing 5 g (0.025 moles) of 2-(pyrrolidin-1-yl)carbonyl-3-hydroxy piperidine, with 1.2 g (0.025 moles) of LiAlH4 in 100 ml of dry THF, using an alkaline work-up, 3 g of the title compound were obtained.
Sources & evidence
- ORD record
- ord-98091e3b26e94aea9f31ab0b98eec4a9
- Source dataset
- uspto-grants-1992_02
- Patent number
- US05089507
Reaction notes
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