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Hydrochloric Acid → 2-(Piperidin-4-yloxy)pyridine dihydrochloride

HRID 23952
Notes
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Reaction equation

HRID 23952 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][N:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:21]>C(OCC)(=O)C>[ClH:21].[ClH:21].[N:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[O:14][CH:11]1[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 219060391-Boc-4-(2-pyridyloxy)piperidine

Product 1

HCID 146741542-(Piperidin-4-yloxy)pyridine dihydrochloride

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

1-t-Butoxycarbonyl-4-(2-pyridoxy)piperidine (6.5 g) was treated with a solution of hydrogen chloride in ethyl acetate (110 ml) for 7 h and the mixture evaporated to give 4-(2-pyridoxy)piperidine dihydrochloride, (7.4 g 90%)

Workup

  1. customthe mixture evaporated

Sources & evidence

ORD record
ord-a5ac776b8b534ee78e46d29a12fb2ac8
Source dataset
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06855715B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes