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HRID 242134Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/242134

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653103B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-14658760966142b38c2ab3a529d1d9dd
Quellennotizuspto-grants-2014_02