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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15863생성일: 2026년 10월 26일

Sodium Carbonate → [2-(Methoxy)-3-nitrophenyl]acetaldehyde

https://huagongshe.com/reaction/15863

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참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Potassium CarbonateHCID 11430—
반응물18-Crown-6HCID 28557—
반응물Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
반응물2-Methoxy-3-nitrobenzaldehydeHCID 14081074—
반응물2-(methoxy)-1-[(E)-2-(methoxy)ethenyl]-3-nitrobenzeneHCID 57454263—
반응물2-(methyloxy)-1-[(Z)-2-(methyloxy)ethenyl]-3-nitrobenzeneHCID 68427638—
용매Hydrochloric AcidHCID 313—
용매TetrahydrofuranHCID 8028—
생성물[2-(Methoxy)-3-nitrophenyl]acetaldehydeHCID 5744434454%

반응 조건

온도60 °C

반응 단계

To a stirred solution of 2-(methoxy)-3-nitrobenzaldehyde in THF were added 18-Crown-6 (0.2 eq), (methoxymethyl)triphenylphosphonium chloride (2 eq) and potassium carbonate (6.5 eq). The resulting suspension was warmed to 60° C. for 2 hours then cooled to room temperature and filtered. The filtrate was concentrated under vacuum and purified by chromatography on a silica cartridge (eluent cyclohexane-ethyl acetate, 9:1) to give a mixture of 2-(methoxy)-1-[(E)-2-(methoxy)ethenyl]-3-nitrobenzene and 2-(methyloxy)-1-[(Z)-2-(methyloxy)ethenyl]-3-nitrobenzene. The alkene mixture was dissolved in THF and 6N hydrochloric acid (1:1), and stirred for 1 hour. The solution was made basic with aqueous sodium carbonate solution and extracted with DCM. The organic layer was washed (water, brine), dried (sodium sulfate) and concentrated under vacuum to give the title compound (54% overall yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732600B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ecd9381d4e544e7cbe61b573e5005ff4
출처 메모uspto-grants-2010_06