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HRID 1532560作成日:2026年10月27日

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

https://huagongshe.com/reaction/1532560

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25 °C

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06204221B1
出典データセットuspto-grants-2001_03
ORD IDord-d29fa9fbecd24dc2b9ef39ec3d0cf1e9
出典メモuspto-grants-2001_03