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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1260908생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1260908

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Diethyl OxalateHCID 7268—
반응물Potassium CarbonateHCID 11430—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 3,4-dichlorophenylacetateHCID 2737422—
용매EthanolHCID 702—
용매M-XyleneHCID 7929—
생성물Ethyl 2-(3,4-dichlorophenyl)acrylateHCID 6887172271%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08470816B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-11372bb424614079a4c3aaf91b641a85
출처 메모uspto-grants-2013_06