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25892-08-4

25892-08-4 Structure

25892-08-4 Structure
IdentificationBack Directory
[Name]

N1-(2,6-DIFLUORO-3-NITROPHENYL)ACETAMIDE
[CAS]

25892-08-4
[Synonyms]

N-(2,6-Difluoro-3-nitrophenyl)
N-(2,6-Difluoro-3-nitrophenyl)acetaMid
N-(2,6-DIFLUORO-3-NITROPHENYL)ACETAMIDE
N1-(2,6-DIFLUORO-3-NITROPHENYL)ACETAMIDE
Acetamide, N-(2,6-difluoro-3-nitrophenyl)-
N1-(2,6-difluoro-3-nitrophenyl)acetamide 95+%
[Molecular Formula]

C8H6F2N2O3
[MDL Number]

MFCD00174326
[MOL File]

25892-08-4.mol
[Molecular Weight]

216.14
Chemical PropertiesBack Directory
[Melting point ]

148 °C
[Boiling point ]

352.7±42.0 °C(Predicted)
[density ]

1.513±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

12.03±0.70(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2924297099
Spectrum DetailBack Directory
[Spectrum Detail]

N1-(2,6-DIFLUORO-3-NITROPHENYL)ACETAMIDE(25892-08-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2',6'-Difluoroacetanilide

3896-29-5

N1-(2,6-DIFLUORO-3-NITROPHENYL)ACETAMIDE

25892-08-4

1. cool sulfuric acid (53.3 mL, 760 mmol) in an ice-water bath and slowly add nitric acid (25.6 mL, 610 mmol), keeping the temperature below 10°C. 2. add N-(2,6-difluorophenyl)acetamide (13.0 g, 76.0 mmol) to the mixed acid solution. 2. N-(2,6-difluorophenyl)acetamide (13.0 g, 76.0 mmol) was added to the above mixed acid solution in batches, ensuring that the reaction temperature was maintained at room temperature. 3. The reaction mixture was stirred at room temperature for 18 hours to carry out the nitration reaction. 4. Upon completion of the reaction, the mixture was slowly poured into ice water to precipitate a yellow solid. 5. The precipitate was collected by filtration and the solid residue was washed well with cold water. 6. The product was dried over air to give 2,6-difluoro-3-nitro-acetanilide (11.2 g, 51.8 mmol, 68% yield) as a yellow solid. 7. The product was analyzed by LCMS (1:1). 7. The product was characterized by LCMS (ESI, cationic mode): calculated C8H6F2N2O3 [M+H]+ 216.0, measured 217.2. 8. 1H NMR (ESI, cationic mode) was performed on the product. 8. 1H NMR (300 MHz, DMSO-d6) δ ppm: 10.04 (br s, 1H, NH), 8.02-8.28 (m, 1H, ArH), 7.44 (td, J = 9.1, 1.8 Hz, 1H, ArH), 2.11 (s, 3H, CH3).

[References]

[1] Journal of Chemical Research, 2004, # 10, p. 699 - 701
[2] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 10, p. 2215 - 2234
[3] Patent: WO2012/85127, 2012, A1. Location in patent: Page/Page column 39
[4] Patent: WO2012/101238, 2012, A1. Location in patent: Page/Page column 38
[5] Patent: US2012/322803, 2012, A1. Location in patent: Page/Page column 17
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