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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 372923생성일: 2026년 10월 26일

1-Bromo-4-fluorobenzene → 2-(4-Fluorophenyl)-5-[(tetra-hydro-2-pyranyloxy)methyl]pyridine

https://huagongshe.com/reaction/372923

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참여 물질

역할이름HCID투입량
반응물1-Bromo-4-fluorobenzeneHCID 9993—
반응물MagnesiumHCID 5462224—
반응물2-Chloro-5-{[(oxan-2-yl)oxy]methyl}pyridineHCID 22127378—
촉매Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chlorideHCID 21654969—
용매TetrahydrofuranHCID 8028—
생성물2-(4-Fluorophenyl)-5-[(tetra-hydro-2-pyranyloxy)methyl]pyridineHCID 1981259777.7%

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온도3 °C

반응 단계

A grignard reagent solution prepared from 1.53 g of magnesium, 10.5 g of 1-bromo-4-fluorobenzene and 70 ml of tetrahydrofuran was added dropwise at 3°-7° C. within 45 minutes to a mixture of 16.9 g of crude 2-chloro-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine, 60 ml of tetrahydrofuran and 0.62 g of 1,3-bis(diphenylphosphino)-propanenickel-(II) chloride. The dark reaction mixture was stirred at 3° C. for a further 1 hr. and at room temperature for 2 hrs. and then extracted with 200 ml of diethyl ether and 120 ml of 0.5N ammonium chloride solution. The organic phase was washed neutral with water, dried over sodium sulphate, filtered and concentrated. Chromatographic purification of the residue on 230 g of silica gel with hexane/ethyl acetate (vol. 9:1) yielded 13.4 g of 2-(4-fluorophenyl)-5-[(tetra-hydro-2-pyranyloxy)methyl]pyridine as a yellowish oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05160661
출처 데이터셋uspto-grants-1992_11
ORD IDord-01403faf49f2441c9fe1f5aa642fa0aa
출처 메모uspto-grants-1992_11