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2-Fluoro-4-(methylsulfonyl)aniline

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2-Fluoro-4-(methylsulfonyl)aniline Basic information

Product Name:
2-Fluoro-4-(methylsulfonyl)aniline
Synonyms:
  • 2-Fluoro-4-(methylsulfonyl)phenylamine
  • 2-Fluoro-4-(methylsulfonyl)aniline
  • 2-Fluoro-4-(methylsulphonyl)aniline 99%
  • 4-Amino-3-fluorophenyl methyl sulphone
  • 2-fluoro-4-(Methylsulfonyl)benzenaMine
  • 2-fluoro-4-Methanesulfonylaniline
  • 1-Amino-2-fluoro-4-(methylsulphonyl)benzene
  • Benzenamine, 2-fluoro-4-(methylsulfonyl)-
CAS:
832755-13-2
MF:
C7H8FNO2S
MW:
189.21
Product Categories:
  • Benzene series
  • API intermediates
  • Amines and Anilines
  • Boron, Nitrile, Thio,& TM-Cpds
Mol File:
832755-13-2.mol
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2-Fluoro-4-(methylsulfonyl)aniline Chemical Properties

Melting point:
145-147°C
Boiling point:
371.0±42.0 °C(Predicted)
Density 
1.374±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
crystalline solid
pka
-0.04±0.10(Predicted)
color 
Faint brown
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2921420090
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2-Fluoro-4-(methylsulfonyl)aniline Usage And Synthesis

Synthesis

29632-74-4

20277-69-4

832755-13-2

The general procedure for the synthesis of 2-fluoro-4-methylsulfinylaniline from 2-fluoro-4-iodoaniline and sodium methanesulfinic acid was as follows: firstly, to a solution of 2-fluoro-4-iodoaniline (206.8 g, 872.3 mmol) in DMSO (1.1 L) was added, in order, copper(II)-benzene trifluoromethanesulfonate complex (30.74 g, 61.1 mmol), sodium methanesulfinic acid ( 106.9 g, 1.047 mol) and N,N'-dimethylethylenediamine (13.2 mL, 122 mmol). Subsequently, the reaction vessel was placed in an oil bath preheated to 120°C and the reaction mixture was stirred overnight. Upon completion of the reaction, the mixture was cooled to room temperature, diluted with water and extracted several times with EtOAc. The organic extracts were combined, washed five times with brine, dried over MgSO4 and concentrated under reduced pressure to remove the solvent. The resulting purple solid was washed with diisopropyl ether and then dried in a vacuum oven at room temperature to constant weight to give 151.5 g of dark purple solid in 92% yield. The product was identified by 1H NMR (DMSO-d6): δ 7.41 (d, 1H, J = 8.5 Hz), 6.87 (t, 1H, J = 8.6 Hz), 6.19 (s, 2H), 3.10 (s, 3H); MS m/z 190.3 (M+).

References

[1] Patent: WO2005/121121, 2005, A2. Location in patent: Page/Page column 148-149

2-Fluoro-4-(methylsulfonyl)aniline Preparation Products And Raw materials

Raw materials

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