| Identification | More | [Name]
5-Fluoro-2-nitroanisole | [CAS]
448-19-1 | [Synonyms]
4-FLUORO-2-METHOXY-1-NITROBENZENE
5-FLUORO-2-NITROANISOL
5-FLUORO-2-NITROANISOLE
5-Fluoro-2-nitroanisole99% | [EINECS(EC#)]
675-631-3 | [Molecular Formula]
C7H6FNO3 | [MDL Number]
MFCD00077541 | [Molecular Weight]
171.13 | [MOL File]
448-19-1.mol |
| Chemical Properties | Back Directory | [Melting point ]
49-51°C | [Boiling point ]
272°C(lit.) | [density ]
1.321±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
powder to crystal | [color ]
White to Amber | [InChI]
InChI=1S/C7H6FNO3/c1-12-7-4-5(8)2-3-6(7)9(10)11/h2-4H,1H3 | [InChIKey]
WLKUSVNHZXUEFO-UHFFFAOYSA-N | [SMILES]
C1([N+]([O-])=O)=CC=C(F)C=C1OC | [CAS DataBase Reference]
448-19-1(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Uses]
3-Fluoro-6-nitroanisole is a reagent used in the synthetic preparation of imidazopyridines as inhibitors of insulin-like growth factor-1 receptor. | [Synthesis]
In a 5L four-necked flask, 2500 g of N,N-dimethylformamide (DMF), 5-fluoro-2-nitrophenol (500 g, 3.20 mol) and anhydrous potassium carbonate (483 g, 3.50 mol) were added and the mixture was heated up to 60 °C. Dimethyl sulfate (424 g, 3.36 mol) was slowly added dropwise for a controlled period of 2-3 hours. After the dropwise addition, the reaction temperature was raised to 90-100 °C and the reaction was maintained for 5-6 hours. The reaction progress was monitored by gas chromatography (GC) until the content of 5-fluoro-2-nitrophenol was below 0.5%. The reaction mixture was cooled to 50 °C, at which point the monomethyl potassium sulfate salt precipitated. The filtrate was subjected to decompression distillation to recover DMF, resulting in 2-nitro-5-fluoroanisole (515 g, yellow oily liquid). The product was analyzed by GC with 99.5% purity and 94.1% yield. | [References]
[1] Chemical and Pharmaceutical Bulletin, 1991, vol. 39, # 9, p. 2323 - 2332
[2] Patent: CN106083536, 2016, A. Location in patent: Paragraph 0035; 0036
[3] Heterocycles, 1992, vol. 34, # 12, p. 2301 - 2311
[4] Patent: WO2010/71885, 2010, A1. Location in patent: Page/Page column 443
[5] Patent: WO2010/115688, 2010, A1. Location in patent: Page/Page column 146 |
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