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3-Bromo-5-fluoro-2-methylaniline

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3-Bromo-5-fluoro-2-methylaniline Basic information

Product Name:
3-Bromo-5-fluoro-2-methylaniline
Synonyms:
  • 3-Bromo-5-fluoro-2-methylaniline
  • 3-Bromo-5-fluoro-2-methylbenzenamine
  • 3-Bromo-5-fluoro-2-methylphenylamine
  • BenzenaMine, 3-broMo-5-fluoro-2-Methyl-
  • 2-Methyl-3-bromo-5-fluoroaniline
  • 2-Amino-6-bromo-4-fluorotoluene 98%
  • 3-Bromo-5-fluoro-2-methylaniline ISO 9001:2015 REACH
CAS:
502496-36-8
MF:
C7H7BrFN
MW:
204.04
Product Categories:
  • Intermediate
Mol File:
502496-36-8.mol
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3-Bromo-5-fluoro-2-methylaniline Chemical Properties

Boiling point:
259℃
Density 
1.589
Flash point:
110℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
2.36±0.10(Predicted)
form 
powder
color 
Light orange to light brown
InChI
InChI=1S/C7H7BrFN/c1-4-6(8)2-5(9)3-7(4)10/h2-3H,10H2,1H3
InChIKey
DSYSVUWIAUMZDQ-UHFFFAOYSA-N
SMILES
C1(N)=CC(F)=CC(Br)=C1C
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Safety Information

HS Code 
2921490090
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3-Bromo-5-fluoro-2-methylaniline Usage And Synthesis

Synthesis

502496-33-5

502496-36-8

General procedure for the synthesis of 2-methyl-3-bromo-5-fluoroaniline from 2-bromo-4-fluoro-6-nitrotoluene: [00402] Ammonium chloride (571 mg, 10.7 mmol) was added to a mixture of 1-bromo-5-fluoro-2-methyl-3-nitrobenzene (500 mg, 2.14 mmol) and iron powder (0.6 g, 10.68 mmol). Water (24 mL) and ethanol (24 mL) were subsequently added. The reaction mixture was refluxed for 5 h. After completion of the reaction, it was filtered through diatomaceous earth and the filter cake was washed with ethanol (100 mL) and ethyl acetate (100 mL). The organic solvent was removed in vacuum to give an aqueous solution, which was extracted with dichloromethane (3 x 30 mL). The organic layer was separated and concentrated to afford the crude product 3-bromo-5-fluoro-2-methylaniline (390 mg, 1.87 mmol, 87.7% yield), which was analyzed by nuclear magnetic resonance (NMR) and showed good purity and could be used in the next reaction without further purification. [00403] 1H NMR (DMSO-d6): δ 6.60 (dd, J = 2.8 and 8.4 Hz, 1H), 6.42 (dd, J = 2.8 and 11.6 Hz, 1H), 5.54 (bs, 2H), 2.09 (s, 3H).

References

[1] Organic Letters, 2017, vol. 19, # 24, p. 6518 - 6521
[2] Green Chemistry, 2018, vol. 20, # 1, p. 130 - 135
[3] Patent: WO2015/79251, 2015, A1. Location in patent: Paragraph 00402; 00403
[4] Patent: WO2011/130628, 2011, A1. Location in patent: Page/Page column 155
[5] Patent: US2013/102595, 2013, A1. Location in patent: Paragraph 0279; 0280

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