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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24306생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/24306

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Dimethyl-3-nitrobenzeneHCID 6739—
반응물Diethyl OxalateHCID 7268—
반응물Potassium ethoxideHCID 23670592—
용매Diethyl EtherHCID 3283—
생성물2-(2-Methyl-6-nitrophenyl)acetic acidHCID 67511545%

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 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-6e4d00333b5f44c18b0da791bf3f2939
출처 메모uspto-grants-2005_02