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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1874Erstellt: 23. Oktober 2026

Hydrogen Peroxide → 4-t-Butoxy-2,3,6-trifluoro-5-hydroxypyridine

https://huagongshe.com/de/reaction/1874

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktTrimethyl borateHCID 8470—
EduktSodium HydroxideHCID 14798—
EduktLithium diisopropylamideHCID 2724682—
Edukt4-t-Butoxy-2,3,6-trifluoropyridineHCID 10608547—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-t-Butoxy-2,3,6-trifluoro-5-hydroxypyridineHCID 10656587—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A 11.16 g (54.39 mmol) sample of 4-t-butoxy-2,3,6-trifluoropyridine, from Example 253 step b above, was dissolved in 50 mL of THF, and the solution was cooled to -78° C. To this solution was added LDA (65.6 mmol) with stirring for 30 min, during which a solid preciptated. To this mixture was added 7.5 mL of trimethoxyborane, with stirring for 25 min at -78° C. To this mixture was added 10 mL of acetic acid, and the mixture was stirred and allowed to warm to room temperature. Next was added 100 mL of 30% hydrogen peroxide and 100 mL of 2N sodium hydroxide while cooling in an ice bath. The mixture was then stirred at room temperature for 16 hours, and quenched with saturated NH4Cl solution. The mixture was extracted with ether, and the extract was washed with brine and dried over MgSO4. The solvent was removed under vacuum, and the residue was purified by flash chromatography on silica gel, eluting with 1:8 ethyl acetate:hexane. Removal of the solvent gave 9.769 g of the title product as a colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726182
Quelldatensatzuspto-grants-1998_03
ORD IDord-c191750ca7b54fdb8dafaf0853defb9d
Quellennotizuspto-grants-1998_03