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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1505388생성일: 2026년 10월 27일

Hydrochloric Acid → 2-Hydroxy-4-[(5-nitro-2-pyridinyl)oxy]benzonitrile

https://huagongshe.com/reaction/1505388

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-5-nitropyridineHCID 78308—
반응물2,4-DihydroxybenzonitrileHCID 3017520—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물2-Hydroxy-4-[(5-nitro-2-pyridinyl)oxy]benzonitrileHCID 67235535117.3%

반응 조건

온도110 °C

반응 단계

In a vial 2,4-dihydroxybenzonitrile (300 mg, 2.2 mmol), 2-chloro-5-nitropyridine (351.96 mg, 2.22 mmol) and K2CO3 (920 mg, 6.62 mmol) were dissolved in DMF (5 mL). The reaction was heated for 1 hour under microwave irradiations (Set Temperature: 110° C.). The reaction mixture was diluted with Et2O and water, acidified with aqueous 1N HCl until pH=2, the phases were separated and the organics were dried over Na2SO4. The solid was filtered out and the solvent was removed affording crude 2-hydroxy-4-[(5-nitro-2-pyridinyl)oxy]benzonitrile (664 mg) as a brown solid. To a solution of this crude in dry DMF (5 mL) potassium carbonate (460 mg, 3.33 mmol) and isopropyl bromide (313 μL, 3.33 mmol) were added and the reaction mixture was stirred overnight at 50° C. The reaction was diluted with brine (10 mL) and extracted with ethyl acetate (2×20 mL). The organic layer was dried (Na2SO4), filtered and evaporated and the residue was purified by flash chromatography on silica gel (SNAP 25 g) eluting from 100:0 to 75:25 cyclohexane/ethyl acetate affording the title compound (260 mg) as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09216967B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-1e7bbb84f6644a98b8c4cca71f9ea360
출처 메모uspto-grants-2015_12