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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1592418생성일: 2026년 10월 27일

Tetrahydrofuran → 3-(3,5-Difluorophenyl)picolinaldehyde

https://huagongshe.com/reaction/1592418

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참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium CarbonateHCID 10340—
반응물(3,5-Difluorophenyl)boronic acidHCID 2734338—
반응물3-Bromopyridine-2-carbaldehydeHCID 16414231—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물3-(3,5-Difluorophenyl)picolinaldehydeHCID 7174290261%

반응 조건

온도90 °C

반응 단계

To a solution of 3-bromo-pyridine-2-carbaldehyde (1.2 g, 6.45 mmol) dissolved in ethylene glycol dimethyl ether (25 mL), THF(10 mL) and saturated solution of Na2CO3 (9 mL) was added 3,5 difluorophenyl boronic acid (1.12 g, 7.10 mmol). Purge the mixture with Ar gas (10 min). To this mixture was added Pd(PPh3)4 (373 mg, 0.33 mmol) and stir under a positive pressure of Ar at 90° C. for 16 hours. The reaction mixture was quenched with a solution of saturated NaHCO3 (50 mL). Extract with CH2Cl2 (2×50 mL). The combined organic extracts were dried (Na2SO4), filtered, and concentrated in vacuo to afford a light yellow oil. Purification via column chromatography on silica gel (CH2Cl2:MeOH: 80:20, v/v/v) afforded 3-(3,5-difluoro-phenyl)-pyridine-2-carbaldehyde as a white solid (0.86 g, 61%). 1H NMR (CDCl3) δ 6.59 (m, 1H), 6.92 (m, 2H), 7.60 (m, 1H), 7.76 (d, 1H, J=7.5 Hz), 8.88 (d, 1H, J=3.5 Hz), 10.11 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07291631B2
출처 데이터셋uspto-grants-2007_11
ORD IDord-482de6ccce6a44d3864a6e48aaa5050d
출처 메모uspto-grants-2007_11