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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 587107생성일: 2026년 10월 26일

Triphenylphosphine → 3-(1-(2,6-Dichloro-3-fluorophenyl)ethoxy)-2-nitropyridine

https://huagongshe.com/reaction/587107

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Ammonium ChlorideHCID 25517—
반응물3-Hydroxy-2-nitropyridineHCID 27057—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물1-(2,6-Dichloro-3-fluorophenyl)ethan-1-olHCID 16770068—
용매TetrahydrofuranHCID 8028—
생성물3-(1-(2,6-Dichloro-3-fluorophenyl)ethoxy)-2-nitropyridineHCID 46942296100%

반응 단계

To a solution of triphenylphosphine (24.29 g, 92.6 mmol) in THF (dry, 160 mL) was added DIAD (18.23 mL, 92.6 mmol) dropwise at 0° C. under N2. After addition of DIAD, a solution of 1-(2,6-dichloro-3-fluorophenyl)ethanol (13.35 g, 63.86 mmol) and 3-hydroxy-2-nitropyridine (10.29 g, 73.44 mmol) in THF (anhydrous, 160 mL) was added dropwise. The ice-bath was removed and the reaction mixture was allowed to warm to room temperature and stirred at room temperature for 4 hrs. The reaction mixture was concentrated by evaporator to give a yellow residue. A saturated solution of NH4Cl (200 mL) was added. The aqueous phase was extracted with EtOAc (3×150 mL). The combined organic phase was washed with brine (2×80 mL), dried over anhydrous Na2SO4, concentrated by evaporation in vacuo to give a yellow residue which was purified by CombiFlash (220 g silica gel column, Hexane/EtOAc) to afford (±)-3-(1-(2,6,-dichloro-3-fluorophenyl)ethoxy)-2-nitropyridine (21.1 g, 100%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09226923B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-a2ecf4d52c2c47388b14afcbde413e15
출처 메모uspto-grants-2016_01