Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402555Erstellt: 26. Oktober 2026

Phthalic Anhydride → 2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxide

https://huagongshe.com/reaction/402555

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalic AnhydrideHCID 6811—
EduktSodium CarbonateHCID 10340—
EduktSodium SulfiteHCID 24437—
EduktCarbamide PeroxideHCID 31294—
Edukttert-Butyl 3-(3-methylpyridin-2-yl)benzoateHCID 57516851—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxideHCID 5848837195%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

tert-Butyl-3-(3-methylpyridin-2-yl)benzoate (1.0 eq) was dissolved in EtOAc (6 vol). Water (0.3 vol) was added, followed by urea-hydrogen peroxide (3 eq). Phthalic anhydride (3 eq) was then added portionwise to the mixture as a solid at a rate to maintain the temperature in the reactor below 45° C. After completion of the phthalic anhydride addition, the mixture was heated to 45° C. After stirring for an additional 4 hours, the heat was turned off. 10% w/w aqueous Na2SO3 (1.5 eq) was added via addition funnel. After completion of Na2SO3 addition, the mixture was stirred for an additional 30 minutes, and the layers separated. The organic layer was stirred, and 10% wt/wt aqueous. Na2CO3 (2 eq) was added. After stirring for 30 minutes, the layers were allowed to separate. The organic phase was washed 13% w/v aq NaCl. The organic phase was then filtered and concentrated to afford crude 2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide (95%) that was used directly in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08742122B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-c7d12dac8bdc4577808ab3df38b69548
Quellennotizuspto-grants-2014_06