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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1051125생성일: 2026년 10월 26일

Nitric Acid → 2-Hydroxy-5-nitro-3-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1051125

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Sulfuric AcidHCID 1118—
반응물2(1H)-Pyridinone, 3-(trifluoromethyl)-HCID 3678411—
용매WaterHCID 962—
용매Sodium HydroxideHCID 14798—
생성물2-Hydroxy-5-nitro-3-(trifluoromethyl)pyridineHCID 2775095—

반응 조건

온도90 °C

반응 단계

A mixture of 3-(trifluoromethyl)pyridin-2(1H)-one 2 (2.00 g, 12.26 mmol) and sulfuric acid (H2SO4, 3.5 ml, 30%) was heated to 90° C. and nitric acid (HNO3, 2.5 ml, 65%) was added. The mixture was stirred at 90° C. for 8 hours and additional nitric acid (1 ml, 65%) was added. The mixture was stirred for an additional 6 hours at 90° C. and was then poured into a beaker containing ice (30 ml). The mixture was diluted with water (30 ml) and 6N aqueous NaOH was added until a pH of about 4 to about 5. The mixture was extracted with ethyl acetate (3×40 ml), the combined organic phases dried over Na2SO4 and all solvents were removed under reduced pressure. The residue was dissolved in ethyl acetate and the product precipitated by the addition of hexane. After filtration, 5-nitro-3-(trifluoromethyl)pyridin-2(1H)-one 3 was obtained as a yellow powder (1.58 g, 7.59 mmol, 62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09388159B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-9daa77167ab74f28bbceb73ec1975f88
출처 메모uspto-grants-2016_07