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| | 1-BroMo-2,5-difluoro-3-nitrobenzene Basic information |
| Product Name: | 1-BroMo-2,5-difluoro-3-nitrobenzene | | Synonyms: | -BroMo-2,5-difluoro-3-nitrobenzene;1-BroMo-2,5-difluoro-3-nitrobenzene;3-BroMo-2,5-difluoronitrobenzene;2,5-Difluoro-3-nitrobromobenzene;Benzene, 1-bromo-2,5-difluoro-3-nitro-;2,5-Difluoro-3-bromonitrobenzene;1-BroMo-2,5-difluoro-3-nitrobenzene ISO 9001：2015 REACH;Carbonodithioicacid,O-ethylester,potassiumsalt(1:4) | | CAS: | 741721-51-7 | | MF: | C6H2BrF2NO2 | | MW: | 237.99 | | EINECS: | | | Product Categories: | | | Mol File: | 741721-51-7.mol |  |
| | 1-BroMo-2,5-difluoro-3-nitrobenzene Chemical Properties |
| Boiling point | 257℃ | | density | 1.890 | | Fp | 109℃ | | storage temp. | 2-8°C | | form | liquid | | color | Clear, pale amber / lime | | InChI | InChI=1S/C6H2BrF2NO2/c7-4-1-3(8)2-5(6(4)9)10(11)12/h1-2H | | InChIKey | ROLNDFKAQIUDIV-UHFFFAOYSA-N | | SMILES | C1(Br)=CC(F)=CC([N+]([O-])=O)=C1F |
| | 1-BroMo-2,5-difluoro-3-nitrobenzene Usage And Synthesis |
| Uses | 1-Bromo-2,5-difluoro-3-nitrobenzene is a nitrobenzene compound containing bromine and fluorine substituents on its benzene ring structure, which can be used as a chemical reaction reagent or organic synthesis intermediate. | | Synthesis | A mixed solution was prepared from 2,5-difluoro-3-nitrobenzoic acid and 3,6-difluoro-2-nitrobenzoic acid (2.48 g, 12.2 mmol, molar ratio 2:1) in carbon tetrachloride (60 mL). Mercury(II) oxide (red, 5.2 g, 24 mmol) was added to this solution and the reaction was carried out at room temperature. Subsequently, the reaction mixture was heated to reflux and reacted under light conditions. Bromine (3.8 g, 24 mmol) was slowly added dropwise to the reaction mixture over a period of 10 min. The reaction mixture was continued under reflux conditions for 6 hours. After completion of the reaction, it was cooled to room temperature and filtered to remove the solid insoluble material. The filtrate was washed sequentially with saturated sodium bicarbonate solution and water. After the solvent was removed by distillation under reduced pressure, the residue was purified by column chromatography (eluent: hexane/ethyl acetate, 8:1, v/v) to afford the target product 2,5-difluoro-3-bromonitrobenzene. The yield was 1.07 g in 38%. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 7.76 (ddd, 1H), 7.64 (ddd, 1H). | | References | [1] Patent: WO2004/69832, 2004, A2. Location in patent: Page 134 |
| | 1-BroMo-2,5-difluoro-3-nitrobenzene Preparation Products And Raw materials |
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