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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24503생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Dimethyl-3-nitrobenzeneHCID 6739—
반응물Diethyl OxalateHCID 7268—
반응물Potassium ethoxideHCID 23670592—
용매Diethyl EtherHCID 3283—
생성물1-Methyl-6-nitrophenylacetic acidHCID 6941901545%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-12261c0d24034cff929a4cc419d10b95
출처 메모uspto-grants-2005_02