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HRID 1260908作成日:2026年10月26日

Formaldehyde → Ethyl 2-(3,4-dichlorophenyl)acrylate

https://huagongshe.com/reaction/1260908

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Diethyl OxalateHCID 7268—
反応物Potassium CarbonateHCID 11430—
反応物Sodium hydrideHCID 24758—
反応物Ethyl 3,4-dichlorophenylacetateHCID 2737422—
溶媒EthanolHCID 702—
溶媒M-XyleneHCID 7929—
生成物Ethyl 2-(3,4-dichlorophenyl)acrylateHCID 6887172271%

反応手順

To a solution of sodium hydride (60% in oil, 6.56 g) in m-xylene (100 mL) was slowly added ethanol (15.7 mL) at 0° C. and then diethyl oxalate (32.0 g) was added. Furthermore, a solution of ethyl 3,4-dichlorophenylacetate (51.0 g) in m-xylene (30 mL) was added at 0° C., and the mixture was stirred at room temperature for 14 hr. To the reaction mixture was added 37% aqueous formalin solution (140 mL) at room temperature, and the mixture was stirred at room temperature for 1 hr. Furthermore, potassium carbonate (115 g) was added at room temperature, and the mixture was stirred at room temperature for 1 hr. The insoluble material was filtered off, and the filtrate was partitioned between ethyl acetate (500 mL) and water (500 mL). The organic layer was separated, washed with brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent; 5% ethyl acetate/hexane) to give crude ethyl 2-(3,4-dichlorophenyl)acrylate (38.1 g, 44%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08470816B2
出典データセットuspto-grants-2013_06
ORD IDord-11372bb424614079a4c3aaf91b641a85
出典メモuspto-grants-2013_06