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| | 6-Nitrophthalide Basic information |
| | 6-Nitrophthalide Chemical Properties |
| Melting point | 140-145 °C(lit.) | | Boiling point | 311.63°C (rough estimate) | | density | 1.4908 (rough estimate) | | refractive index | 1.5160 (estimate) | | storage temp. | Sealed in dry,Room Temperature | | form | Crystalline Powder | | color | Pale yellow | | Water Solubility | 0.4g/L(25 ºC) | | CAS DataBase Reference | 610-93-5(CAS DataBase Reference) |
| | 6-Nitrophthalide Usage And Synthesis |
| Chemical Properties | pale yellow crystalline powder | | Uses | 6-Nitrophthalide is a fluorescent heterocycle that can be used as a probe for specific inhibition. It is homologous to other fluorescent probes such as fluorescein, nitrobenzene, and nitrophenol. It has been shown to have inhibitory properties against triazole and dipole, which are catalytic asymmetric. 6-Nitrophthalide has also been shown to have the ability to inhibit the oxidation of aldehydes. | | Preparation | 6-Nitrophthalide is synthesized from 2-nitrobenzaldehyde via a two-step process, and then reacted with methyl iodide. | | Application | 6-Nitrophthalide has been used in the preparation of 3-bromo-6-nitrophthalide. It undergoes reductive methylation to form 6-dimethylaminophthalide. | | Synthesis | Step A: Synthesis of 6-nitrobenzofuran-1(3H)-one
1. dissolve phthalide (40.0 g, 298 mmol) in sulfuric acid (50.0 mL) under ice bath conditions and stir until homogeneous.
2. dissolve potassium nitrate (30.4 g, 300 mmol) in sulfuric acid (80 mL) and add to the above sulfuric acid solution of phthalide by dropping.
3. Keeping the reaction mixture under stirring, the reaction mixture was slowly warmed up to room temperature, which took about 5 hours.
4. Upon completion of the reaction, the mixture was slowly poured into ice water to precipitate.
5. The precipitate was collected and recrystallized from ethanol (3 L) to give 6-nitrobenzofuran-1(3H)-one (50.4 g, 94% yield) as an off-white solid.
6. The structure and purity (98%) of the product were confirmed by nuclear magnetic resonance hydrogen spectroscopy (1H NMR, 500 MHz, CDCl3) with the following characteristic peaks: δ 8.77 (d, J = 1.5 Hz, 1H), 8.58 (dd, J = 8.5, 2.0 Hz, 1H), 7.72 (d, J = 8.5 Hz, 1H), 5.45 (s, 2H). | | References | [1] Journal fuer Praktische Chemie/Chemiker-Zeitung, 1993, vol. 335, # 1, p. 17 - 22
[2] Patent: WO2012/142459, 2012, A1. Location in patent: Page/Page column 37
[3] Journal of Heterocyclic Chemistry, 1992, vol. 29, # 6, p. 1519 - 1523
[4] Patent: US2008/9524, 2008, A1. Location in patent: Page/Page column 409
[5] Patent: US2011/98311, 2011, A1 |
| | 6-Nitrophthalide Preparation Products And Raw materials |
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