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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1187506Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1187506

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
Edukt2,2,2-Trifluoro-1-methoxyethanolHCID 9892—
EduktPotassium CarbonateHCID 11430—
Edukt5-hydroxy-2-methyl-1H-pyridin-4-one hydrochlorideHCID 67282658—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt3-hydroxy-6-methyl-2-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-oneHCID 25018652—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08673943B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-1c57b5b7bae44642a79a4332b6b8f588
Quellennotizuspto-grants-2014_03