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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 650476생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/650476

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

온도110 °C

반응 단계

An autoclave is charged with 200 g of 2,3-dichloro-5-trifluoromethylpyridine, 1.85 liters of ethanol, 260 ml of triethylamine and 6.5 g of palladium bis(triphenylphosphine) dichloride (PdCl2(PPh3)2). At 25° C. a pressure of 110 bars is then applied with carbon monoxide and the mixture is maintained 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 of 0.035 mbar. 200 g of the desired product are obtained in the form of a yellow oil having a boiling point of 67-70° C./0.035 mbar (yield 85% of the theoretical yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06274536B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-046dd745272d4d8daefffc6dca8299b2
출처 메모uspto-grants-2001_08