| Identification | Back Directory | [Name]
2,6-DIFLUORO-4-IODOANILINE | [CAS]
141743-49-9 | [Synonyms]
BUTTPARK 120\07-58
2,6-DIFLUORO-4-IODOANILINE
2,6-Difluoro-4-iodioaniline
2,6-Difluoro-4-iodoaniline 98%
BenzenaMine,2,6-difluoro-4-iodo-
2,6-Difluoro-4-iodine-phenylamine | [Molecular Formula]
C6H4F2IN | [MDL Number]
MFCD07774189 | [MOL File]
141743-49-9.mol | [Molecular Weight]
255 |
| Chemical Properties | Back Directory | [Melting point ]
77-79°C | [Boiling point ]
223℃ | [density ]
2.086 | [Fp ]
89℃ | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [form ]
Solid | [pka]
1.02±0.10(Predicted) | [Appearance]
White to light brown Solid |
| Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 2,6-difluoro-4-iodoaniline from 2,6-difluoroaniline is as follows: 2,6-difluoroaniline (3.0 g, 22.56 mmol) was dissolved in acetic acid (10 mL). To this solution iodine monochloride (3.581 g, 22.56 mmol) was added. The reaction mixture was stirred at room temperature for 15 minutes. After completion of the reaction, the solvent was removed by evaporation and the residue was neutralized with aqueous sodium carbonate. Subsequently, the aqueous phase was extracted with dichloromethane. The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and the solvent evaporated to afford the target product 2,6-difluoro-4-iodoaniline in 95% yield. | [References]
[1] Journal of the American Chemical Society, 2012, vol. 134, # 51, p. 20597 - 20600
[2] Patent: WO2004/74266, 2004, A1. Location in patent: Page 54
[3] Patent: WO2006/15985, 2006, A1. Location in patent: Page/Page column 54
[4] Journal of Organic Chemistry, 2009, vol. 74, # 19, p. 7370 - 7382
[5] European Journal of Organic Chemistry, 2010, # 16, p. 3049 - 3067 |
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