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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1532560생성일: 2026년 10월 26일

Ethanol → Ethyl 3-chloro-5-(trifluoromethyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/1532560

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물TriethylamineHCID 8471—
반응물2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
반응물HCID 178418416HCID 178418416—
촉매Bis(triphenylphosphine)palladium chlorideHCID 84124—
생성물Ethyl 3-chloro-5-(trifluoromethyl)pyridine-2-carboxylateHCID 2201355885%

반응 조건

온도25 °C

반응 단계

An autoclave is loaded with 200 g of 2,3-dichloro-5-trifluoromethylpyridine, 1.85 l of ethanol, 260 ml of triethylamine and 6.5 g of palladium bis(triphenylphosphine)dichloride (PdCl2(PPh3)2). 110 bar of carbon monoxide are then forced in at 25° C. and the mixture is kept at 110° C. for 24 hours. After cooling to 25° C., the crude mixture is concentrated to a thick slurry, which is then partitioned between dilute sodium chloride solution and ethyl acetate. After extraction by shaking and separation of the phases, the ethyl acetate phase is washed with water, dried over sodium sulfate and concentrated to dryness. The crude product is distilled under a high vacuum at 0.035 mbar. 200 g of the desired product are obtained as a yellow oil of boiling point 67-70° C./0.035 mbar (yield 85% of theory)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06204221B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-d29fa9fbecd24dc2b9ef39ec3d0cf1e9
출처 메모uspto-grants-2001_03