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HRID 650476作成日:2026年10月25日

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

https://huagongshe.com/reaction/650476

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物TriethylamineHCID 8471—
反応物2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
反応物HCID 178418416HCID 178418416—
触媒Bis(triphenylphosphine)palladium chlorideHCID 84124—
生成物Ethyl 3-chloro-5-(trifluoromethyl)pyridine-2-carboxylateHCID 2201355885%

反応条件

温度110 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06274536B1
出典データセットuspto-grants-2001_08
ORD IDord-046dd745272d4d8daefffc6dca8299b2
出典メモuspto-grants-2001_08