Basic information Safety Supplier Related

2-FLUORO-6-METHOXYANILINE

Basic information Safety Supplier Related

2-FLUORO-6-METHOXYANILINE Basic information

Product Name:
2-FLUORO-6-METHOXYANILINE
Synonyms:
  • 2-FLUORO-6-METHOXYANILINE
  • 2-fluoro-6-methoxybenzenamine
  • 2-Amino-3-fluoroanisole, 6-Fluoro-o-anisidine
  • 2-AMino-3-fluoroanisole[2-Fluoro-6-Methoxyaniline]
  • 2-Fluoro-6-methoxy-phenylamine
  • -FLUORO-6-METHOXYANILINE
  • Benzenamine, 2-fluoro-6-methoxy-
CAS:
446-61-7
MF:
C7H8FNO
MW:
141.14
Mol File:
446-61-7.mol
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2-FLUORO-6-METHOXYANILINE Chemical Properties

Boiling point:
208 °C(Press: 756 Torr)
Density 
1.176±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
3.15±0.10(Predicted)
form 
slightly viscous liquid
color 
Clear, peach/khaki
InChI
InChI=1S/C7H8FNO/c1-10-6-4-2-3-5(8)7(6)9/h2-4H,9H2,1H3
InChIKey
VHHKZASLPJMWJI-UHFFFAOYSA-N
SMILES
C1(N)=C(OC)C=CC=C1F
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22
Hazard Note 
Irritant
HS Code 
2922290090
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2-FLUORO-6-METHOXYANILINE Usage And Synthesis

Chemical Properties

black liquid

Synthesis

641-49-6

446-61-7

General procedure for the synthesis of 2-fluoro-6-methoxyaniline using 3-fluoro-2-nitroanisole as starting material: 10% Pd/C catalyst (7.46 g, 70.1 mmol) and ethanol (400 mL) were added to a Parr reactor followed by 1-fluoro-3-methoxy-2-nitrobenzene (40.0 g, 234 mmol). The reactor was evacuated and filled with hydrogen (50 psi) and the reaction was shaken for 5 h under hydrogen atmosphere. After completion of the reaction, the catalyst was removed by Celite filtration and the filtrate was concentrated to give 2-fluoro-6-methoxyaniline (30.0 g, 83% yield) as a colorless oil. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 3.75 (broad single peak, 2H), 3.86 (single peak, 3H), 6.58-6.71 (multiple peaks, 3H); the molecular ion peak [M + H]+ = 142 was detected by LC-MS (LC-ES).

References

[1] Patent: WO2018/69863, 2018, A1. Location in patent: Page/Page column 248
[2] Journal of the American Chemical Society, 1932, vol. 54, p. 2973,2976
[3] Journal of the Chemical Society, 1931, p. 981
[4] Journal of Medicinal Chemistry, 1993, vol. 36, # 11, p. 1641 - 1653

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