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HRID 913042作成日:2026年10月24日

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

https://huagongshe.com/reaction/913042

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物2,2,2-Trifluoro-1-methoxyethanolHCID 9892—
反応物Potassium CarbonateHCID 11430—
反応物5-hydroxy-2-methyl-1H-pyridin-4-one hydrochlorideHCID 67282658—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物3-hydroxy-6-methyl-2-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-oneHCID 25018652—

反応条件

温度100 °C

反応手順

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° 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08026261B2
出典データセットuspto-grants-2011_09
ORD IDord-7b1e6d08f0f8468cbe07850641faef23
出典メモuspto-grants-2011_09