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| | 2-Fluoro-4-nitrobenzoic acid Basic information | | Application |
| | 2-Fluoro-4-nitrobenzoic acid Chemical Properties |
| Melting point | 170 °C | | Boiling point | 352.5±27.0 °C(Predicted) | | density | 1.568±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | pka | 2.37±0.13(Predicted) | | form | powder to crystal | | color | White to Light yellow | | BRN | 2582091 | | InChI | InChI=1S/C7H4FNO4/c8-6-3-4(9(12)13)1-2-5(6)7(10)11/h1-3H,(H,10,11) | | InChIKey | MMWFMFZFCKADEL-UHFFFAOYSA-N | | SMILES | C(O)(=O)C1=CC=C([N+]([O-])=O)C=C1F | | CAS DataBase Reference | 403-24-7(CAS DataBase Reference) |
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ALFA
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| | 2-Fluoro-4-nitrobenzoic acid Usage And Synthesis |
| Application | 2-Fluoro-4-nitrobenzoic acid is a raw material for the synthesis of enzalutamide, mainly used in laboratory pharmaceutical research and development. | | Chemical Properties | white to light yellow crystal powder | | Synthesis | A mixture of 2-fluoro4-nitrotoluene (31.1 g, 0.2 mol), tetrabutylammonium bromide (3.2 g,0.01 mol), 1.0 L of 1N NaOH, and KMnO4 (20.0 g) was stirred at room temperature. After 10 min, the resulting mixture was heated to 95 °Cwith stirring. Additional 30.0 g portions of KMnO 4 were added after 2 h and 3 h. After stirring at 95 °C for an additional 10 h, the reaction mixture was cooled to room temperature and filtered through Celite to remove MnO2. The filtrate was acidified to pH 2 by adding concentrated hydrochloric acid. An off-white precipitate formed that was collected by vacuum filtration. The crude solid was dissolved in 300 mL of 1N aqueous NaOH, acidified to pH 2 using concentrated hydrochloric acid, and the mixture extracted with CH 2 Cl 2 (3 × 200 mL). The combined CH2 Cl 2extracts were washed with 0.1 N aqueous HCl (2 × 100 mL), dried over anhydrous Na2SO4, and concentrated in vacuo to afford 27.3 g (73.7%)of 2-fluoro-4-nitrobenzoic acid as a white crystalline solid, m.p. 174.5–176.0 °C (lit 7. m.p. 176–177 °C)[1].
| | References | [1] Defeng Xu, Zhiling Zhu, Xing Xu. “A Convenient Synthesis of 4-amino-2-fluoro-N-methyl-benzamide.” Journal of Chemical Research-s 17 1 (2013): 615–616.
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| | 2-Fluoro-4-nitrobenzoic acid Preparation Products And Raw materials |
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