참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Salicylic Acid | HCID 338 | — |
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | 2-Chloro-4-nitroaniline | HCID 8492 | — |
| 반응물 | Phosphorus trichloride | HCID 24387 | — |
| 생성물 | N-(2-chloro-4-nitrophenyl)-2 hydroxybenzamide | HCID 2844786 | — |
반응 단계
The method disclosed in U.S. Pat. No. 3,079,297 to Shraufstatter et al with minor variations was utilized. A boiling solution of salicylic acid (1.03 g, 7.46 mmol) and 2-chloro-4-nitroaniline (1.29 g, 7.46 mmol) in xylenes (20 mL) was treated dropwise with a solution of phosphorous trichloride in dichloromethane 2.0M, 1.50 mL, 0.40 equiv.), and the resulting solution was refluxed (137° C.) for four hours. The solution was cooled to about 125° C. An oily residue covered the bottom and sides of the reaction vessel. The hot reaction solution was transferred by glass pipette to a beaker and was allowed to cool to room temperature while being stirred rapidly. The product separated, was collected by filtration, and washed with hexanes, then recrystallized from ethanol. The title compound was obtained, MP 218-220° C. (dec.). 1HNMR (500 MHz, DMSO-d6): δ 7.02 (m, 1H, H3), 7.07 (m, 1H, H5), 7.49 (m, 1H, H4), 8.04 (m, 1H, H6), 8.28 (m, 1H, H5′), 8.41 (m, 1H, H3′), 8.85 (m, 1H, H6′), 11.8 (s, 1H, NH), 12.34 (s, 1H, OH).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08211882B2 |
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| 출처 데이터셋 | uspto-grants-2012_07 |
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| ORD ID | ord-f7371c5d6ddf4995b96f3264db1f0942 |
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| 출처 메모 | uspto-grants-2012_07 |
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