5-Fluoro-2-nitroanisole CAS 448-19-1

Introduction:Basic information about 5-Fluoro-2-nitroanisole CAS 448-19-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

5-Fluoro-2-nitroanisole Basic information

Product Name:5-Fluoro-2-nitroanisole
Synonyms:2-Nitro-5-Fluoro Anisole;1-Fluoro-3-Methoxy-4-nitrobenzene;uoro-2-methoxy-1-nitrobenzene;Anisole, 5-fluoro-2-nitro- (8CI);4-Fluoro-2-methoxy-1-nitrobenzene, 5-Fluoro-2-nitrophenyl methyl ether;4-Fluoro-2-Methoxy-1-nitrobenzene, 95+%;5 - fluoro - 2 - nitrobenzene Methyl ether;Benzene, 4-fluoro-2-methoxy-1-nitro-
CAS:448-19-1
MF:C7H6FNO3
MW:171.13
EINECS:675-631-3
Product Categories:Fluorine series;blocks;NitroCompounds;API
Mol File:448-19-1.mol

5-Fluoro-2-nitroanisole Chemical Properties

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
InChIInChI=1S/C7H6FNO3/c1-12-7-4-5(8)2-3-6(7)9(10)11/h2-4H,1H3
InChIKeyWLKUSVNHZXUEFO-UHFFFAOYSA-N
SMILESC1([N+]([O-])=O)=CC=C(F)C=C1OC
CAS DataBase Reference448-19-1(CAS DataBase Reference)

Safety Information

Hazard Codes Xi,Xn
Risk Statements 22-52
HazardClass IRRITANT
HS Code 2909309090

5-Fluoro-2-nitroanisole Usage And Synthesis

Uses3-Fluoro-6-nitroanisole is a reagent used in the synthetic preparation of imidazopyridines as inhibitors of insulin-like growth factor-1 receptor.
Synthesis

446-36-6

77-78-1

448-19-1

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

5-Fluoro-2-nitroanisole Preparation Products And Raw materials

Raw materials5-Fluoro-2-nitrophenol-->4-FLUORO-2-METHOXYANILINE-->2-(tert-butoxy)-4-fluoro-1-nitrobenzene-->Iodomethane-->Potassium carbonate-->2,4-Difluoronitrobenzene-->3-Fluoroanisole-->2,4-Dimethoxy-1-nitrobenzene-->Dimethyl sulfate-->Methanol
Preparation Products3-Fluoro-4-nitroanisole
5-Fluoro-2-methoxyaniline CAS 1978-39-8
5-Fluoro-2-oxindole CAS 56341-41-4
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