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1-Methylimidazole → HCID 131719089, compound

HRID 1757056
Notes
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Reaction equation

HRID 1757056 reaction equation
C(=O)([O-])[O-].[Co+2:5].[CH:6](=[O:14])[C:7]1[C:8](=[CH:10][CH:11]=[CH:12][CH:13]=1)[OH:9].[CH3:15][N:16]1[CH:20]=[CH:19][N:18]=[CH:17]1>>[CH3:15][N:16]1[CH:20]=[CH:19][N:18]=[CH:17]1.[CH3:15][N:16]1[CH:20]=[CH:19][N:18]=[CH:17]1.[Co+2:5].[CH:6](=[O:14])[C:7]1[C:8](=[CH:10][CH:11]=[CH:12][CH:13]=1)[OH:9].[CH:6](=[O:14])[C:7]1[C:8](=[CH:10][CH:11]=[CH:12][CH:13]=1)[OH:9]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 13901-MethylimidazoleHCID 6998SalicylaldehydeHCID 10565Cobaltous carbonate

Product 1

HCID 131719089HCID 131719089, compoundYield 97%

Procedure

1 mole of cobalt (II) carbonate was thoroughly mixed with 2 moles of salicylaldehyde with an excess of 1-methyl imidazole at moderate temperatures using the procedure of Example 1 to obtain a 97% yield of bis-(salicylaldehyde)-cobalt (II) di(1-methylimidazole)

Sources & evidence

ORD record
ord-ae1f7ea938cc4857adccff19448cce16
Source dataset
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05444030

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes