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HRID 1161492作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/1161492

反応式

関与物質

役割名称HCID仕込み量
反応物N-FormylmorpholineHCID 20417—
反応物Ammonium ChlorideHCID 25517—
反応物2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocyclohepteneHCID 59517213—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物4-Methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene-2-carbaldehydeHCID 59517047—

反応条件

温度-70 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07816522B2
出典データセットuspto-grants-2010_10
ORD IDord-e0b48d1b5945417c8e033d5c1089acc4
出典メモuspto-grants-2010_10