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Oxygen → 4-Chlorobenzoic Acid

HRID 9750
Notes
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Reaction equation

HRID 9750 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.ON1C(=O)N(O)C(=O)N(O)[C:11]1=[O:20].[O:21]=O>C([O-])(=O)C.[Co+2].C([O-])(=O)C.C(O)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:11]([OH:20])=[O:21])=[CH:4][CH:3]=1.[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 977OxygenHCID 78104-ChlorotolueneHCID 104197231,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trione

Product 2

HCID 63184-Chlorobenzoic AcidHCID 78104-Chlorotoluene

Reagents, catalysts & solvents 2

HCID 6277Cobalt diacetateCatalyst
On this pageParticipantsProcedureSources & evidenceReaction notes
HCID 176
Acetic Acid
Solvent

Procedure

A mixture of 0.380 g of 4-chlorotoluene, 0.027 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (5% by mole relative to 4-chlorotoluene), 5 g of acetic acid and 0.004 g of cobalt(II) acetate.4H2O was stirred at 100° C. in an atmosphere of oxygene gas (1 atm=0.1 MPa) for 14 hours. The resulting product in the reaction mixture was analyzed by gas chromatography and was found to yield 4-chlorobenzoic acid in 99% yield at 100% conversion of 4-chlorotoluene.

Sources & evidence

ORD record
ord-c6a8ba3d36bf4f319c6bd44ce0526ecd
Source dataset
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07091342B2

Reaction notes

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