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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553355Generated: October 30, 2026

Diethyl Ether → 4-Nitro-o-toluic acid

https://huagongshe.com/reaction/553355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHexaneHCID 8058—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Iodo-3-nitrotolueneHCID 234781—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Nitro-o-toluic acidHCID 7479031.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1.0 g (3.8 mmol) of 2-iodo-nitrotoluene, 2.1 g (15.2 mmol) potassium carbonate and 27 mg (0.038 mmol) of palladium(II) dichloride bis(triphenylphosphine) in a mixture of 5 mL of water and 10 mL of N,N-dimethylformamide. This was placed in a Fisher/Porter bottle under 15 psig of carbon monoxideand heated at 70° C. for 16 hours. The solution became homogeneous when heated. The reaction was cooled, diethyl ether and water was added, the organic layer separated and discarded. The aqueous layer was acidified with IN hydrohloric acid, extracted with ethyl acetate, washed with water, brine, dried over magnesium sulfate, filtered and concentrated to yield 0.5 g of crude material. This dissolved in ethyl acetate, hexane added and the resulting brown solid discarded. The filtrate was concentrated, and then recrystallized fom diethyl ether/hexane to afford 215 mg of 4-nitro-2-methylbenzoic acid, m/e=182 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE042889E1
Source datasetuspto-grants-2011_11
ORD IDord-2e69f8efd29f484b93949c4b6aa97162
Source noteuspto-grants-2011_11