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HRID 734583作成日:2026年10月25日

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

https://huagongshe.com/reaction/734583

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物Potassium CarbonateHCID 11430—
反応物18-Crown-6HCID 28557—
反応物Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
反応物2-Methoxy-3-nitrobenzaldehydeHCID 14081074—
反応物2-(methoxy)-1-[(E)-2-(methoxy)ethenyl]-3-nitrobenzeneHCID 57454263—
反応物2-(methyloxy)-1-[(Z)-2-(methyloxy)ethenyl]-3-nitrobenzeneHCID 68427638—
溶媒Hydrochloric AcidHCID 313—
溶媒TetrahydrofuranHCID 8028—
生成物[2-(Methoxy)-3-nitrophenyl]acetaldehydeHCID 5744434454%

反応条件

温度60 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07592346B2
出典データセットuspto-grants-2009_09
ORD IDord-9cf2842c80454b048fcca439efe68889
出典メモuspto-grants-2009_09