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HRID 402555생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/402555

반응식

참여 물질

역할이름HCID투입량
반응물Phthalic AnhydrideHCID 6811—
반응물Sodium CarbonateHCID 10340—
반응물Sodium SulfiteHCID 24437—
반응물Carbamide PeroxideHCID 31294—
반응물tert-Butyl 3-(3-methylpyridin-2-yl)benzoateHCID 57516851—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxideHCID 5848837195%

반응 조건

온도45 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08742122B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-c7d12dac8bdc4577808ab3df38b69548
출처 메모uspto-grants-2014_06