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Potassium Carbonate → Diazo bis-(4-chloro-phenyl)-methane

HRID 257812
Notes
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Reaction equation

HRID 257812 reaction equation
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([C:6](=[N:14][NH2:15])[C:7]2[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.S([O-])([O-])(=O)=O.[Mg+2].C(=O)([O-])[O-].[K+].[K+]>C(Cl)Cl.[Ag]=O>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([C:7]2[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=2)=[N+:14]=[N-:15])=[CH:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 11430Potassium CarbonateHCID 24083Sulfuric acid magnesium salt (1:1)HCID 224202Bis(4-chlorophenyl)methylidenehydrazine

Product 1

HCID 11323003Diazo bis-(4-chloro-phenyl)-methane

Reagents, catalysts & solvents 2

HCID 92152Silver(II) oxideCatalyst
HCID 6344
Dichloromethane
Solvent

Procedure

To a stirred ice-cold solution of 4,4'-dichlorobenzophenone hydrazone (1.303 g) in dry methylene chloride (20 ml) was added magnesium sulfate (590 mg), silver oxide (1.196 g) was added in one portion followed by potassium carbonate (30 mg). The mixture was stirred at ice-temperature for 1 hour, then at room temperature for an additional hour, filtered through Celite to give a dark purple solution which was directly used for the cycloaddition reaction.

Workup

  1. additionwas added in one portion
  2. waitat room temperature for an additional hour
  3. filtrationfiltered through Celite
  4. customto give a dark purple solution which
  5. customwas directly used for the cycloaddition reaction

Sources & evidence

ORD record
ord-44f5373d2a204d62bb072eaeceaa1a57
Source dataset
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05264430

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes