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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1187506생성일: 2026년 10월 27일

Carbon Dioxide → 3-hydroxy-6-methyl-2-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one

https://huagongshe.com/reaction/1187506

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물2,2,2-Trifluoro-1-methoxyethanolHCID 9892—
반응물Potassium CarbonateHCID 11430—
반응물5-hydroxy-2-methyl-1H-pyridin-4-one hydrochlorideHCID 67282658—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물3-hydroxy-6-methyl-2-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-oneHCID 25018652—

반응 단계

5-Hydroxy-2-methyl-1H-pyridin-4-one hydrochloride (1.00 g, 6.19 mmol) and potassium carbonate (1.02 g, 7.42 mmol) was mixed together in water (10 mL) at room temperature, and stirred until evolution of carbon dioxide ceased. Then, 2,2,2-trifluoro-1-methoxy-ethanol (1.60 g, 12.4 mmol) was added. The reaction mixture was heated in a sealed flask at 100.degree. C. for 20 h. The mixture was cooled down to RT and neutralized with acetic acid to pH at between 5 to 6. The precipitate was collected by suction filtration and washed with water and ether. Thus, 3-hydroxy-6-methyl-2-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one was obtained as an off-white solid (1.06 g, 76% yield). 1H NMR (90 MHz, DMSO-d6) δ (ppm): 6.09 (s, 1H, CH); 5.42 (apparent q, 1H, CH), 2.28 (s, 3H, CH3); MS-ESI (m/z) 224.1 [M+1]+, 206.1, 186.1, 178.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673943B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-1c57b5b7bae44642a79a4332b6b8f588
출처 메모uspto-grants-2014_03