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HRID 24503作成日:2026年10月24日

1,2-Dimethyl-3-nitrobenzene → 1-Methyl-6-nitrophenylacetic acid

https://huagongshe.com/ja/reaction/24503

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Dimethyl-3-nitrobenzeneHCID 6739—
反応物Diethyl OxalateHCID 7268—
反応物Potassium ethoxideHCID 23670592—
溶媒Diethyl EtherHCID 3283—
生成物1-Methyl-6-nitrophenylacetic acidHCID 6941901545%

反応手順

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 refluxed for 0.5 hr, concentrated, and treated with 10% sodium hydroxide until almost all of the solid dissolved. Hydrogen peroxide (30%) was then added to the dark red mixture 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 1-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 4-methyl-2-oxindole as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855730B2
出典データセットuspto-grants-2005_02
ORD IDord-12261c0d24034cff929a4cc419d10b95
出典メモuspto-grants-2005_02