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79110-05-7

79110-05-7 Structure

79110-05-7 Structure
IdentificationBack Directory
[Name]

1-(2-Fluoro-5-nitrophenyl)ethan-1-one
[CAS]

79110-05-7
[Synonyms]

2'-Fluoro-5'-nitroacetophenone 96%
1-(2-Fluoro-5-nitrophenyl)ethanone
Ethanone,1-(2-fluoro-5-nitrophenyl)-
1-(2-Fluoro-5-nitrophenyl)ethan-1-one
1-(2-Fluoro-5-nitrophenyl)ethan-1-one ISO 9001:2015 REACH
1-(2-Fluoro-5-nitrophenyl)ethan-1-one, 3-Acetyl-4-fluoronitrobenzene
[EINECS(EC#)]

639-356-2
[Molecular Formula]

C8H6FNO3
[MDL Number]

MFCD00277867
[MOL File]

79110-05-7.mol
[Molecular Weight]

183.137
Chemical PropertiesBack Directory
[Melting point ]

53-54 °C
[Boiling point ]

241.0±20.0 °C(Predicted)
[density ]

1.336±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[color ]

White to Yellow to Green
[InChI]

InChI=1S/C8H6FNO3/c1-5(11)7-4-6(10(12)13)2-3-8(7)9/h2-4H,1H3
[InChIKey]

BCXOSCQTHVTUET-UHFFFAOYSA-N
[SMILES]

C(=O)(C1=CC([N+]([O-])=O)=CC=C1F)C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[HS Code ]

2914790090
Hazard InformationBack Directory
[Uses]

2''-Fluoro-5''-nitroacetophenone
[Synthesis]

2'-Fluoroacetophenone

445-27-2

1-(2-Fluoro-5-nitrophenyl)ethan-1-one

79110-05-7

A solution of 1-(2-fluorophenyl)ethanone (90.0 g, 652 mmol) with fuming nitric acid (53.1 mL) in concentrated sulfuric acid (129 mL) was slowly added dropwise to concentrated sulfuric acid (360 mL, 93-98%) pre-cooled to -42 °C under mechanical stirring. The reaction mixture was kept stirred at -42°C for 30 minutes. Upon completion of the reaction, the mixture was slowly poured into ice (1.3 kg) to quench the reaction. Subsequently, water (1 L) was added to precipitate the product from the solution. After all the ice melted, the precipitate was collected by filtration. The resulting solid was dissolved in EtOAc and the organic layer was washed sequentially with 5% aqueous Na2CO3 (2 x 300 mL), water (1 x 300 mL) and brine (1 x 300 mL), dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated to give a yellow solid 1-(2-fluoro-5-nitrophenyl)ethanone (115 g, 97% yield).

[References]

[1] Patent: WO2012/139425, 2012, A1. Location in patent: Page/Page column 117
[2] Patent: WO2011/44184, 2011, A1. Location in patent: Page/Page column 99-100
[3] Patent: US2004/122237, 2004, A1. Location in patent: Page 388
[4] Journal of Heterocyclic Chemistry, 1991, vol. 28, # 3, p. 673 - 683
[5] Patent: US2002/151715, 2002, A1
Spectrum DetailBack Directory
[Spectrum Detail]

1-(2-Fluoro-5-nitrophenyl)ethan-1-one(79110-05-7)1HNMR
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