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1220886-29-2

1220886-29-2 Structure

1220886-29-2 Structure
IdentificationBack Directory
[Name]

4-BroMo-5-fluoro-2-nitro-benzoic acid Methyl ester
[CAS]

1220886-29-2
[Synonyms]

Methyl 4-broMo-5-fluoro-2-nitrobenzoate
3-Bromo-2-fluoro-6-nitro-benzoic acid methyl ester
4-BroMo-5-fluoro-2-nitro-benzoic acid Methyl ester
Benzoic acid, 4-bromo-5-fluoro-2-nitro-, methyl ester
[Molecular Formula]

C8H5BrFNO4
[MDL Number]

MFCD21606583
[MOL File]

1220886-29-2.mol
[Molecular Weight]

278.03
Chemical PropertiesBack Directory
[Boiling point ]

337.6±42.0 °C(Predicted)
[density ]

1.742±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to yellow Solid
[InChI]

InChI=1S/C8H5BrFNO4/c1-15-8(12)4-2-6(10)5(9)3-7(4)11(13)14/h2-3H,1H3
[InChIKey]

HPMNCYDJGIMYKN-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)C1=CC(F)=C(Br)C=C1[N+]([O-])=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H302-H319-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
Spectrum DetailBack Directory
[Spectrum Detail]

4-BroMo-5-fluoro-2-nitro-benzoic acid Methyl ester(1220886-29-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-nitro-4-Bromo-5-fluorobenzoic acid

1020717-99-0

Iodomethane

74-88-4

4-BroMo-5-fluoro-2-nitro-benzoic acid Methyl ester

1220886-29-2

Potassium carbonate (5.870 g, 42.47 mmol) was slowly added to a stirred solution of 4-bromo-5-fluoro-2-nitrobenzoic acid (Ark Pharm, 5.387 g, 20.40 mmol) in N,N-dimethylformamide (DMF, 80.0 mL) at 0 °C, followed by dropwise addition of iodomethane (8.789 g, 61.92 mmol). The reaction mixture was stirred at 0 °C for 15 min and then gradually warmed up to 40 °C and maintained for 2 hours. After completion of the reaction, the mixture was filtered and concentrated. The concentrated residue was dissolved in ethyl acetate (EtOAc, 150 mL), washed sequentially with water (2 x 100 mL) and saturated brine (100 mL), and the organic phase was dried with anhydrous sodium sulfate (Na2SO4), and concentrated under reduced pressure to remove the solvent. The crude product obtained was purified by fast column chromatography on silica gel with the eluent being hexane solution of 0-50% ethyl acetate to give methyl 4-bromo-5-fluoro-2-nitrobenzoate as a light yellow oil (5.348 g, 94% yield). Liquid chromatography-mass spectrometry (LCMS) analysis: theoretically calculated value for C8H6BrFNO4 ([M+H]+): m/z = 277.9; no ionization was observed.

[References]

[1] Patent: US2014/200216, 2014, A1. Location in patent: Paragraph 0485; 0486
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