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HRID 1870作成日:2026年10月24日

Iodoethane → 2-Propyl-3,4,5,6-tetrafluoropyridine

https://huagongshe.com/ja/reaction/1870

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物HexaneHCID 8058—
反応物Lithium diisopropylamideHCID 2724682—
反応物2,3,4,5-Tetrafluoro-6-methylpyridineHCID 15388342—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-Propyl-3,4,5,6-tetrafluoropyridineHCID 19691283—

反応条件

温度-60 °C

反応手順

A 1.5M solution of LDA in hexane (100 mL, 150 mmol) is cooled to -60° C. in an isopropyl alcohol/dry ice bath. To the stirred LDA solution, under nitrogen, is added, dropwise over a 0.5 hours period, a solution of 22.617 g (137 mmol) of 3,4,5,6-tetrafluoro-2-picoline, the product of Step 1, in 80 mL of dry THF. The reaction mixture is stirred for 0.5 hours at -60° C. and then a solution of 10.95 mL (137 mmol) of ethyl iodide in 30 mL of dry THF is added, dropwise over a 20 minute period. After the reaction mixture is stirred at -60° C. for 0.5 hours, the cooling bath is allowed to slowly (1.5 hours) warm to -30° C. The reaction mixture is poured into cold brine and the aqueous mixture is extracted with methylene chloride. The organic extract is dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue is distilled to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726182
出典データセットuspto-grants-1998_03
ORD IDord-487343b7458b49df9d5c356386d96e9c
出典メモuspto-grants-1998_03