참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 2,3,5-Trimethyl-1-oxidopyridin-1-ium | HCID 10486907 | — |
| 용매 | Sulfuric Acid | HCID 1118 | — |
| 생성물 | 4-Nitro-2,3,5-trimethylpyridine, 1-oxide | HCID 11217611 | — |
반응 단계
65 ml of fuming nitric acid (d =1.5) are added dropwise to 210 ml of conc. sulphuric acid while cooling. 96.5 g of 2,3,5-trimethylpyridine 1-oxide are subsequently added portionwise at 0°-5°, whereupon the mixture is stirred at room temperature for 1 hour, then heated to 90° within 3 hours and left at this temperature overnight. After cooling the solution is poured on to 1.5 kg of ice, whereupon the mixture is adjusted to pH 3 with conc. sodium hydroxide solution and extracted three times with 500 ml of methylene chloride. The combined organic phases are washed with 1 1 of water, dried over sodium sulphate and evaporated in vacuo. The residue is crystallized from ether/petroleum ether and there is obtained 2,3,5-trimethyl-4-nitropyridine 1-oxide of melting point 76°-78°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04766133 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-8696c6546cb4490a8cc107f0fb9d9507 |
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| 출처 메모 | uspto-grants-1988_08 |
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