참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phthalic Anhydride | HCID 6811 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | Sodium Sulfite | HCID 24437 | — |
| 반응물 | Carbamide Peroxide | HCID 31294 | — |
| 반응물 | tert-Butyl 3-(3-methylpyridin-2-yl)benzoate | HCID 57516851 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxide | HCID 58488371 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08742122B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-c7d12dac8bdc4577808ab3df38b69548 |
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| 출처 메모 | uspto-grants-2014_06 |
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