ChemicalBook--->CAS DataBase List--->448-19-1

448-19-1

448-19-1 Structure

448-19-1 Structure
IdentificationMore
[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 PropertiesBack 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)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H341
[Precautionary statements ]

P201-P202-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P308+P313-P405-P501
[Hazard Codes ]

Xi
[Risk Statements ]

22-52
[Hazard Note ]

Irritant
[REACH Registrations]

Active
[HazardClass ]

IRRITANT
[HS Code ]

2909309090
Hazard InformationBack 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]

5-Fluoro-2-nitrophenol

446-36-6

Dimethyl sulfate

77-78-1

5-Fluoro-2-nitroanisole

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
Spectrum DetailBack Directory
[Spectrum Detail]

5-Fluoro-2-nitroanisole(448-19-1)1HNMR
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