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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402555Generated: October 25, 2026

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

https://huagongshe.com/reaction/402555

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) 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742122B2
Source datasetuspto-grants-2014_06
ORD IDord-c7d12dac8bdc4577808ab3df38b69548
Source noteuspto-grants-2014_06