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5,6-Dihydroquinoline → 5,6,7,8-Tetrahydro-7-dimethylaminoquinoline

HRID 1461293
Notes
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Reaction equation

HRID 1461293 reaction equation
[Cl-].[CH3:2][NH2+:3][CH3:4].[N:5]1[C:14]2[CH:13]=[CH:12][CH2:11][CH2:10][C:9]=2[CH:8]=[CH:7][CH:6]=1>>[CH3:2][N:3]([CH3:4])[CH:12]1[CH2:13][C:14]2[N:5]=[CH:6][CH:7]=[CH:8][C:9]=2[CH2:10][CH2:11]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 123183175,6-DihydroquinolineHCID 12954980Dimethylazanium;chloride

Product 1

HCID 148359225,6,7,8-Tetrahydro-7-dimethylaminoquinoline

Procedure

This compound was prepared from dimethylammonium chloride (1.63 g, 20 mmol) and 5,6-dihydroquinoline (1.31 g, 10 mmol) using the experimental and purification method describes in Example 48. The product (0.72 g) was an oil which was identical to the compound isolated in Example 3.

Workup

  1. custompurification method

Sources & evidence

ORD record
ord-8cf27b10e2d64258a70bc63b4b0d63ed
Source dataset
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05075303

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes