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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 425909생성일: 2026년 10월 24일

Triphenylphosphine → 3-(2,6-Dichloro-3-fluoro-benzyloxy)-2-nitro-pyridine

https://huagongshe.com/ko/reaction/425909

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-Hydroxy-2-nitropyridineHCID 27057—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물1-(2,6-Dichloro-3-fluorophenyl)ethan-1-olHCID 16770068—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물3-(2,6-Dichloro-3-fluoro-benzyloxy)-2-nitro-pyridineHCID 21111399100%

반응 단계

To a stirred solution of triphenyl phosphine (8.2 g, 0.03 mol) and DEAD (13.65 mL of a 40% solution in toluene) in THF (200 mL) at 0° C. was added a solution of 1-(2,6-dichloro-3-fluoro-phenyl)-ethanol (4.55 g, 0.021 mol) and 3-hydroxy-nitropyridine (3.35 g, 0.023 mol) in THF (200 mL). The resulting bright orange solution was stirred under a nitrogen atmosphere at ambient temperature for 4 hours at which point all starting materials had been consumed. The solvent was removed, and the crude material was dry loaded onto silica gel, and eluted with ethyl acetate-hexanes (20:80) to yield 3-(2,6-dichloro-3-fluoro-benzyloxy)-2-nitro-pyridine (6.21 g, 0.021 mol, 98%) as a pink solid. 1H NMR (CDCl3, 300 MHz) δ1.8-1.85 (d, 3H), 6.0-6.15 (q, 1H), 7.0-7.1 (t, 1H), 7.2-7.21 (d, 1H), 7.25-7.5 (m, 2H), 8.0-8.05 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08106197B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-bf20a6a3a4aa434eb0322700e183425a
출처 메모uspto-grants-2012_01