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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1698738생성일: 2026년 10월 27일

N-Formylmorpholine → 4-Methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene-2-carbaldehyde

https://huagongshe.com/reaction/1698738

반응식

참여 물질

역할이름HCID투입량
반응물N-FormylmorpholineHCID 20417—
반응물Ammonium ChlorideHCID 25517—
반응물2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocyclohepteneHCID 59517213—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-Methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene-2-carbaldehydeHCID 59517047—

반응 조건

온도-70 °C

반응 단계

To a solution of 420 mg of 2-bromo-4-methoxy-8,9-dihydro-5,7-dioxa-benzocycloheptene in 10 ml of THF there was added dropwise 0.7 ml of n-butyllithium (2.66 M, hexane solution) at −70° C. under a nitrogen atmosphere. After stirring at −70° C. for 10 minutes, 0.5 ml of N-formylmorpholine was added and the temperature was raised from −70° C. to 0° C. over a period of 30 minutes. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (235 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163787B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-dc6960bf1c9e4c31abc9c0b7d433fc03
출처 메모uspto-grants-2012_04