참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | 2-methoxypyridine N-oxide hydrochloride | HCID 12562076 | — |
| 용매 | Sulfuric Acid | HCID 1118 | — |
| 생성물 | 2-Methoxy-4-nitropyridine-n-oxide | HCID 579207 | — |
반응 단계
30 ml of concentrated sulfuric acid, cooled to 0° C., are added to 15.5 g of 2-methoxypyridine N-oxide hydrochloride, after which 42 ml of fuming nitric acid and 14 ml of concentrated sulfuric acid are added dropwise at 0° C. After the temperature has been allowed to rise, the reaction mixture is heated for 3 hours at 90°-100° C. and is then cooled and poured onto 50 g of ice. It is neutralized to pH 7 by the addition of concentrated aqueous ammonia at a temperature below 10° C. The aqueous phase is extracted 6 times with methylene chloride, the organic phase is then dried over sodium sulfate and concentrated and 11 g of a yellow solid corresponding to a mixture of 2-methoxy-4-nitropyridine N-oxide and 2-methoxy-5-nitropyridine N-oxide are recovered. The 2 products are separated by chromatography on silica using a methylene chloride/methanol mixture (95/5) as the eluent. 6.3 g of 2-methoxy-4-nitropyridine N-oxide are collected.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05284838 |
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| 출처 데이터셋 | uspto-grants-1994_02 |
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| ORD ID | ord-bd7cf4875ee54beab717671be826d4ec |
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| 출처 메모 | uspto-grants-1994_02 |
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