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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019105Generated: October 25, 2026

1,2-Dimethyl-3-nitrobenzene → 2-(2-Methyl-6-nitrophenyl)acetic acid

https://huagongshe.com/reaction/1019105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dimethyl-3-nitrobenzeneHCID 6739—
ReactantDiethyl OxalateHCID 7268—
ReactantPotassium ethoxideHCID 23670592—
SolventDiethyl EtherHCID 3283—
Product2-(2-Methyl-6-nitrophenyl)acetic acidHCID 67511545%

Reaction Steps

Diethyl oxalate (30 mL) in 20 mL of dry ether was added with stirring to 19 g of potassium ethoxide suspended in 50 mL of dry ether. The mixture was cooled in an ice bath and 20 mL of 3-nitro-o-xylene in 20 mL of dry ether was slowly added. The thick dark red mixture was heated to reflux for 0.5 hr, concentrated to a dark red solid, and treated with 10% sodium hydroxide until almost all of the solid dissolved. The dark red mixture was treated with 30% hydrogen peroxide until the red color changed to yellow. The mixture was treated alternately with 10% sodium hydroxide and 30% hydrogen peroxide until the dark red color was no longer present. The solid was filtered off and the filtrate acidified with 6N hydrochloric acid. The resulting precipitate was collected by vacuum filtration, washed with water, and dried under vacuum to give 9.8 g (45% yield) of 2-methyl-6-nitrophenylacetic acid as an off-white solid. The solid was hydrogenated in methanol over 10% palladium on carbon to give 9.04 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486185B1
Source datasetuspto-grants-2002_11
ORD IDord-b7c4b6c7aa364849aeb0cac29cc9287a
Source noteuspto-grants-2002_11