HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 457621Erstellt: 23. Oktober 2026
1,2-Dimethyl-3-nitrobenzene → 2-(2-Methyl-6-nitrophenyl)acetic acid
https://huagongshe.com/de/reaction/457621
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dimethyl-3-nitrobenzene | HCID 6739 | — |
| Edukt | Diethyl Oxalate | HCID 7268 | — |
| Edukt | Potassium ethoxide | HCID 23670592 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2-(2-Methyl-6-nitrophenyl)acetic acid | HCID 675115 | 45% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07189721B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-1b357ea44aa14af49a859711da1567b3 |
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| Quellennotiz | uspto-grants-2007_03 |
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