참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 반응물 | Methanone, (2-hydroxy-5-nitrophenyl)phenyl- | HCID 519604 | — |
| 용매 | Potassium Hydroxide | HCID 14797 | — |
| 생성물 | 5-Nitro-2-hydroxybenzophenone oxime | HCID 136258108 | — |
반응 단계
Into an autoclave, were charged 30 g of 2-chloro-5-nitrobenzophenone, 300 ml of water, and 9.70 g of potassium hydroxide. The mixture was allowed to react at 150° to 160° C. with stirring for 5 hours. Upon cooling to room temperature, there was obtained a clear liquid, reddish orange in color. The liquid was further cooled below 0° C. and strongly acidified with cold concentrated hydrochloric acid. The precipitated solids were collected by filtration, washed with water, and recrystallized from ethanol to yield 15.7 g (56.1%) of 5-nitro-2-hydroxy-benzophenone having a melting point of 122°-123° C. To 150 ml of 40-% aqueous potassium hydroxide solution, was added 25.0 g of 5-nitro-2-hydroxybenzophenone followed by 50 g of hydroxylamine hydrochloride. After 5 hours, the resulting clear liquid was cooled and acidified with concentrated hydrochloric acid to form a precipitate. The precipitate was washed with water and a small volume of 50-% aqueous methanol, then dried in air, and recrystallized from benzene and petroleum ether to yield 5-nitro-2-hydroxybenzophenone oxime.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04559172 |
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| 출처 데이터셋 | uspto-grants-1985_12 |
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| ORD ID | ord-0a6fdccfed1d47dd8b55cd0832f16062 |
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| 출처 메모 | uspto-grants-1985_12 |
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