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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743035생성일: 2026년 10월 26일

Methanesulfonic Acid → 1-(4-Pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthalene

https://huagongshe.com/reaction/1743035

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물Dimethyl maleateHCID 5271565—
반응물3,4-Dimethoxy-6-(4-pyridyl) hydroxymethylbenzaldehyde dimethylacetalHCID 22007378—
용매Acetic AcidHCID 176—
용매TolueneHCID 1140—
생성물1-(4-Pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthaleneHCID 1172864262.2%

반응 단계

To a solution of 3,4-dimethoxy-6-(4-pyridyl) hydroxymethylbenzaldehyde dimethylacetal (18.4 g) in a mixture of acetic acid (50 ml) and toluene (50 ml) is added dimethyl maleate (8.64 ml), and the mixture is refluxed for one hour. To the mixture is added methanesulfonic acid (9.33 ml), and the mixture is refluxed for 8 hours while removing the resulting water with a Dean-Stalk apparatus. The mixture is cooled to room temperature, and concentrated. The residue is dissolved in chloroform, and the pH value thereof is adjusted with aqueous potassium carbonate solution to pH 8. The mixture is extracted twice with each 100 ml of chloroform, and the extracts are washed with a saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. The resulting residue is crystallized from diethyl ether to give a diester compound, 1-(4-pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthalene (13.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05342941
출처 데이터셋uspto-grants-1994_08
ORD IDord-ea6e579a5bde40b8844841c48e68995a
출처 메모uspto-grants-1994_08