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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182339Generated: October 31, 2026

Acetic Acid → 2-Nitrotoluene

https://huagongshe.com/reaction/1182339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-NitrotolueneHCID 6944—
Reactant1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trioneHCID 10419723—
CatalystCobalt diacetateHCID 6277—
CatalystManganous AcetateHCID 12525—
SolventWaterHCID 962—
Product2-NitrotolueneHCID 6944—
Product2-Nitrobenzoic acidHCID 11087—

Reaction Conditions

Temperature150 °C

Reaction Steps

In an autoclave, 0.274 g of 2-nitrotoluene, 0.018 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (5% by mole relative to 2-nitrotoluene), 5 g of acetic acid, 0.003 g of cobalt(II) acetate.4 H2O, 0.001 g of manganese(II) acetate .4 H2O and 0.018 g of NO2 were placed. The autoclave was charged with 1 MPa of air and placed in a heated oil bath. The mixture was stirred at 150° C. for 14 hours. After the completion of reaction, the autoclave was placed on cold water to cool down the reaction mixture quickly. The resulting mixture was analyzed by gas chromatography and was found to yield 2-nitrobenzoic acid in 62% yield at 67% conversion of 2-nitrotoluene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288649B2
Source datasetuspto-grants-2007_10
ORD IDord-37def8aa7d144b21999200a2c6a7e8ae
Source noteuspto-grants-2007_10