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| | 2-Hydroxy-3-nitroacetophenone Basic information |
| | 2-Hydroxy-3-nitroacetophenone Chemical Properties |
| Melting point | 98.5-99.5 °C | | Boiling point | 223.5±20.0 °C(Predicted) | | density | 1.380±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | pka | 7.31±0.24(Predicted) | | Appearance | Yellow to brown Solid | | InChI | InChI=1S/C8H7NO4/c1-5(10)6-3-2-4-7(8(6)11)9(12)13/h2-4,11H,1H3 | | InChIKey | XQZGSPSZLMKODN-UHFFFAOYSA-N | | SMILES | C(=O)(C1=CC=CC([N+]([O-])=O)=C1O)C | | CAS DataBase Reference | 28177-69-7(CAS DataBase Reference) |
| | 2-Hydroxy-3-nitroacetophenone Usage And Synthesis |
| Preparation | Preparation by reaction of boiling 5% aqueous potassium hydroxide on 8-nitrochromone (78%). | | Synthesis | General procedure for the synthesis of 2-hydroxy-5-nitroacetophenone and 2-hydroxy-3-nitroacetophenone from 2'-hydroxyacetophenone: In a four-necked flask, 2'-hydroxyacetophenone (175 g), acetic acid (183 g), and dichloromethane (800 mL) were added sequentially, and the mixture was heated to 40 °C. Subsequently, 63% concentrated nitric acid (165 g) was slowly added dropwise, and the reaction temperature was controlled to be maintained at 40 °C for 4-6 hours. After completion of the dropwise addition, the reaction was continued at 40 °C for 4-6 hours. At the end of the reaction, water (500 g) was added and stirred for 30 minutes for extraction and layering. The organic layer was concentrated to about 200 g of crude product. The above crude product (200 g) was added to a four-necked flask with toluene (900 g), heated to 60-70 °C and reacted at 70-80 °C for 2-4 hours. The reaction mixture was cooled to 30-50 °C and filtered and the filter cake was dried. The dried filter cake was transferred to a four-necked flask, methanol (100 g) and water (800 g) were added and heated to 50-60°C. The reaction mixture was cooled to 30-50°C and filtered. Acetic acid (150 g) was added slowly dropwise and controlled to be added dropwise within 2 hours at 60-70 °C. The reaction mixture was cooled to room temperature and filtered, and the filter cake was dried to give the product A-2 (80 g). | | References | [1] Journal of Medicinal Chemistry, 1994, vol. 37, # 20, p. 3353 - 3362
[2] Asian Journal of Chemistry, 2015, vol. 27, # 6, p. 2117 - 2124
[3] Patent: WO2009/85256, 2009, A1. Location in patent: Page/Page column 55
[4] Patent: CN103980257, 2016, B. Location in patent: Paragraph 0033; 0034; 0035 |
| | 2-Hydroxy-3-nitroacetophenone Preparation Products And Raw materials |
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