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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1870생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물HexaneHCID 8058—
반응물Lithium diisopropylamideHCID 2724682—
반응물2,3,4,5-Tetrafluoro-6-methylpyridineHCID 15388342—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물2-Propyl-3,4,5,6-tetrafluoropyridineHCID 19691283—

반응 조건

온도-60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726182
출처 데이터셋uspto-grants-1998_03
ORD IDord-487343b7458b49df9d5c356386d96e9c
출처 메모uspto-grants-1998_03