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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242134Generated: October 26, 2026

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

https://huagongshe.com/reaction/242134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantSodium CarbonateHCID 10340—
ReactantSodium SulfiteHCID 24437—
ReactantCarbamide PeroxideHCID 31294—
Reactanttert-Butyl 3-(3-methylpyridin-2-yl)benzoateHCID 57516851—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxideHCID 5848837195%

Reaction Conditions

Temperature45 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653103B2
Source datasetuspto-grants-2014_02
ORD IDord-14658760966142b38c2ab3a529d1d9dd
Source noteuspto-grants-2014_02