Name | 2-Fluoro-4-(methylsulfonyl)aniline |
Synonyms | 2-fluoro-4-Methanesulfonylaniline 2-Fluoro-4-(methylsulfonyl)aniline 4-Amino-3-fluorophenyl methyl sulphone 2-Fluoro-4-(methylsulfonyl)phenylamine 2-fluoro-4-(Methylsulfonyl)benzenaMine Benzenamine, 2-fluoro-4-(methylsulfonyl)- 1-Amino-2-fluoro-4-(methylsulphonyl)benzene |
CAS | 832755-13-2 |
InChI | InChI=1/C7H8FNO2S/c1-12(10,11)5-2-3-7(9)6(8)4-5/h2-4H,9H2,1H3 |
Molecular Formula | C7H8FNO2S |
Molar Mass | 189.21 |
Density | 1.374±0.06 g/cm3(Predicted) |
Melting Point | 145-147°C |
Boling Point | 371.0±42.0 °C(Predicted) |
Flash Point | 178.168°C |
Vapor Presure | 0mmHg at 25°C |
pKa | -0.04±0.10(Predicted) |
Storage Condition | 2-8°C(protect from light) |
Refractive Index | 1.551 |
Hazard Symbols | Xi - Irritant |
Hazard Class | IRRITANT |
Application | 2-fluoro-4-(methylsulfonyl) aniline can be used as intermediates in organic synthesis and pharmaceutical intermediates, mainly used in laboratory research and development process and chemical production process. |
preparation | 2-fluoro-4-iodoaniline (206.8g,872.3mmol) in DMSO(1.1L) copper (II) trifluoromethanesulfonate-benzene complex (30.74g,61.1mmol), sodium methanesulfonate (106.9g,1.047mol) and N,N-dimethylethylenediamine (13.2mL,122mmol). The reaction vessel was then placed in an oil bath preheated to 120 °c and stirred overnight. After cooling to room temperature, the reaction was diluted with water and extracted repeatedly with EtOAc. The combined organic extracts were rinsed with brine (5x), dried over MgSO4, and the solvent removed. The resulting purple solid was rinsed with diisopropyl ether and then dried in a vacuum oven overnight at room temperature to constant weight to give a dark purple solid, 51.5g, yield 92% |