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ChemicalBook--->CAS DataBase List--->98447-30-4

98447-30-4

98447-30-4 Structure

98447-30-4 Structure
IdentificationBack Directory
[Name]

3-BROMO-4-NITROANISOLE
[CAS]

98447-30-4
[Synonyms]

2-Bromo-4-methoxynitrobenzene
3-Methoxy-6-nitrobromobenzene
[Molecular Formula]

C7H6BrNO3
[MDL Number]

MFCD06797977
[MOL File]

98447-30-4.mol
[Molecular Weight]

232.03
Chemical PropertiesBack Directory
[Melting point ]

69℃
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMO-4-NITROANISOLE(98447-30-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Methoxy-2-nitrobenzoic acid

1882-69-5

3-BROMO-4-NITROANISOLE

98447-30-4

General procedure for the synthesis of 3-bromo-4-nitroanisole from 5-methoxy-2-nitrobenzoic acid: silver sulfate (6.2 mg), copper acetate (36.3 mg), 2,9-dimethyl-1,10-o-phenanthroline (12.5 mg), 5-methoxy-2-nitrobenzoic acid (39.4 mg), and sodium bromide (30.9 mg), followed by the addition of 4 mL of dimethyl sulfoxide (DMSO) as solvent. The reaction mixture was heated to 160°C under oxygen atmosphere and stirred for 24 hours. After completion of the reaction, the reaction was quenched by the addition of distilled water and extracted three times with ethyl acetate (10 mL each time). The organic phases were combined and concentrated to afford 3-bromo-4-nitroanisole (20.4 mg) in 44% yield.

[References]

[1] Journal of Organic Chemistry, 2016, vol. 81, # 7, p. 2794 - 2803
[2] Patent: CN107325002, 2017, A. Location in patent: Paragraph 0133
[3] Organic and Biomolecular Chemistry, 2018, vol. 16, # 30, p. 5416 - 5421
[4] Tetrahedron Letters, 2010, vol. 51, # 50, p. 6646 - 6648
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