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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252107Generated: November 1, 2026

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

https://huagongshe.com/reaction/2252107

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 numberUS07320996B2
Source datasetuspto-grants-2008_01
ORD IDord-6d0cb42281444a7ea35aa1b806cd8950
Source noteuspto-grants-2008_01