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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1436085Erstellt: 24. Oktober 2026

Hydrogen Peroxide → 2-Hydroxy-4-(3,4,5-trifluorobenzyl)morpholin-3-one

https://huagongshe.com/de/reaction/1436085

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktSodium HydroxideHCID 14798—
EduktLithium tri-s-butylborohydrideHCID 3611392—
EduktSodium BisulfiteHCID 23665763—
Edukt4-(3,4,5-Trifluorobenzyl)morpholine-2,3-dioneHCID 69010337—
LösungsmittelChloroformHCID 6212—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt2-Hydroxy-4-(3,4,5-trifluorobenzyl)morpholin-3-oneHCID 6900471053%

Reaktionsschritte

A 1 M solution of lithium tri-sec-butylborohydride in THF (31.4 mL) was added dropwise to a solution of 4-(3,4,5-trifluorobenzyl)morpholine-2,3-dione (7.38 g) in THF at −15° C., and the reaction solution was stirred for two hours. A 5 N sodium hydroxide solution (2.85 mL) and 30% aqueous hydrogen peroxide (968 μL) were added dropwise to the reaction solution at 20° C. or less, which was then stirred at 10° C. for one hour. Sodium bisulfite (888 mg) was added to the reaction solution, which was then stirred for 30 minutes. Brine and chloroform were added to the reaction solution, and the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography using a silica gel (heptane:ethyl acetate=1:1 to 0:100) to obtain 3.94 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07618960B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-4b7cdc45b9ec452b93cfd55390b3b84a
Quellennotizuspto-grants-2009_11