HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004671Generated: October 25, 2026
1,2-Dimethyl-3-nitrobenzene → 2-(2-Methyl-6-nitrophenyl)acetic acid
https://huagongshe.com/reaction/1004671
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dimethyl-3-nitrobenzene | HCID 6739 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Methyl-6-nitrophenyl)acetic acid | HCID 675115 | 45% |
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 6 N 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051593 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-ffc4022044bf4323a057e0c8858271a5 |
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| Source note | uspto-grants-2000_04 |
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