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Lithium hydroxide, monohydrate → 1-(3,3-Dimethylbutyl)piperidine-4-carboxylic acid

HRID 220801
Notes
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Reaction equation

HRID 220801 reaction equation
O.[OH-].[Li+].C([O:6][C:7]([CH:9]1[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][C:17]([CH3:20])([CH3:19])[CH3:18])[CH2:11][CH2:10]1)=[O:8])C>C1COCC1.O>[CH3:18][C:17]([CH3:20])([CH3:19])[CH2:16][CH2:15][N:12]1[CH2:13][CH2:14][CH:9]([C:7]([OH:8])=[O:6])[CH2:10][CH2:11]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 168937Lithium hydroxide, monohydrateHCID 606927891-(3,3-Dimethyl-butyl)-piperidine-4-carboxylic Acid Ethyl Ester

Product 1

HCID 231123781-(3,3-Dimethylbutyl)piperidine-4-carboxylic acidYield 87%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

Lithium hydroxide monohydrate (1.37 g, 32.6 mmol) was added to a solution of 1-(3,3-dimethyl-butyl)-piperidine-4-carboxylic acid ethyl ester from Example E15.1 (7.16 g, 29.7 mmol) in THF (50 ml) and water (5 ml). The mixture was stirred at room temperature for 18 h then concentrated in vacuo. The residue was purified by flash chromatography on silica gel through an isolute (eluant; 90% dichloromethane:9% methanol:1% acetic acid) to yield the title compound (5.51 g, 87%).

Workup

  1. concentrationthen concentrated in vacuo
  2. customThe residue was purified by flash chromatography on silica gel through an isolute (eluant; 90% dichloromethane:9% methanol:1% acetic acid)

Sources & evidence

ORD record
ord-38515c25826d4220ab5c47f995f3f5d9
Source dataset
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08202858B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes