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Chemical Structure| 1239462-97-5 Chemical Structure| 1239462-97-5

Structure of 1239462-97-5

Chemical Structure| 1239462-97-5

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Product Details of [ 1239462-97-5 ]

CAS No. :1239462-97-5
Formula : C9H5BrFN
M.W : 226.05
SMILES Code : FC1=CC(Br)=C2C=CC=NC2=C1
MDL No. :MFCD20527915
InChI Key :KIRTXFHNXXGJLP-UHFFFAOYSA-N
Pubchem ID :68755221

Safety of [ 1239462-97-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1239462-97-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1239462-97-5 ]

[ 1239462-97-5 ] Synthesis Path-Downstream   1~5

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  • [ 134168-98-2 ]
  • [ 56-81-5 ]
  • [ 852061-94-0 ]
  • [ 1239462-97-5 ]
YieldReaction ConditionsOperation in experiment
With ferrous(II) sulfate heptahydrate; sulfuric acid; In nitrobenzene; at 80℃; To 3-bromo-5-fluoroaniline hydrochloride (2.9 g, 12.89 mmol) was added glycerol (1.9 mL, 25.99 mmol), nitrobenzene (1.3 mL), sulfuric acid (3.5 mL) and iron (II) sulfate heptahydrate (0.23 g, 0.82 mmol). The reaction mixture was placed in an oil bath set at 80 0C and stirred overnight followed by basification with 12Ν NaOH and extraction with dichloromethane. The organic phase was collected, dried (sodium sulfate), filtered and concentrated under reduced pressure. Purification by flash chromatography (silica, 50:50 ethyl acetate/hexane) gave 5-bromo-7-fluoroquinoline and 7-bromo-5-fluoroquinoline (1.03 g, 30%) Retention time (min) = 1.877 and 1.967, method [4], MS(ESI) 227.9 (M+H).
With ferrous(II) sulfate heptahydrate; sulfuric acid; In nitrobenzene; at 80℃; for 12.0h; 3-Bromo-5-fluoroaniline hydrochloride (4.00 g, 17.66 μMol) and glycerol (3.26 g, 35.50 μMol) were dissolvedin nitrobenzene (2 mL). Iron(II) sulfate heptahydrate (0.24 g, 0.06 μMol) and concentrated sulfuric acid (4.8 mL) wereadded to the solution. The mixture was stirred at 80C for 12 hours. The mixture was cooled to room temperature andneutralized with a saturated aqueous sodium hydrogen carbonate solution. The organic layer was extracted with ethylacetate, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified bysilica gel column chromatography (hexane/ethyl acetate = 95/5 -> 90/10) to obtain a mixture (2.4 g) of compound 127-1-1and compound 127-1-2.ESIMS m/z: [M + H]+ 226.
With ferrous(II) sulfate heptahydrate; sulfuric acid; In nitrobenzene; at 80℃; for 12.0h; 3-Bromo-5-fluoroaniline hydrochloride (4.00 g, 17.66 mmol) and glycerol (3.26 g, 35.50 mmol) were dissolved in nitrobenzene (2 mL). Iron(II) sulfate heptahydrate (0.24 g, 0.06 mmol) and concentrated sulfuric acid (4.8 mL) were added to the solution. The mixture was stirred at 80C for 12 hours. The mixture was cooled to room temperature and neutralized with a saturated aqueous sodium hydrogen carbonate solution. The organic layer was extracted with ethyl acetate, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate = 95/5 -> 90/10) to obtain a mixture (2.4 g) of compound 127-1-1 and compound 127-1-2.
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  • 4
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  • [ 51656-70-3 ]
  • [ 1239462-98-6 ]
  • 5
  • [ 56-81-5 ]
  • [ 134168-97-1 ]
  • [ 1239462-97-5 ]
 

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