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7304-32-7

7304-32-7 Structure

7304-32-7 Structure
IdentificationMore
[Name]

2-Fluoro-5-nitrobenzoic acid
[CAS]

7304-32-7
[Synonyms]

2-FLUORO-5-NITROBENZOIC ACID
BUTTPARK 32\01-76
RARECHEM AL BO 0445
2-Fluoro-5-nitrobenzoic acid 98%
2-Fluoro-5-nitrobenzoicacid98%
2-FLUORO-5-NITRROBENZOIC ACID
2-Fluoro-5-nitrobenzotc acid
[EINECS(EC#)]

627-772-7
[Molecular Formula]

C7H4FNO4
[MDL Number]

MFCD00134238
[Molecular Weight]

185.11
[MOL File]

7304-32-7.mol
Chemical PropertiesBack Directory
[Appearance]

white to light yellow crystal powder
[Melting point ]

142-144 °C (lit.)
[Boiling point ]

337.7±27.0 °C(Predicted)
[density ]

1.568±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

Soluble in chloroform, ethanol.
[form ]

Crystalline Powder
[pka]

2.54±0.10(Predicted)
[color ]

White to pale yellow
[BRN ]

1912835
[InChI]

InChI=1S/C7H4FNO4/c8-6-2-1-4(9(12)13)3-5(6)7(10)11/h1-3H,(H,10,11)
[InChIKey]

ICXSHFWYCHJILC-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC([N+]([O-])=O)=CC=C1F
[CAS DataBase Reference]

7304-32-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29163990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

white to light yellow crystal powder
[Uses]

2-Fluoro-5-nitrobenzoic acid may be used in the synthesis of:
  • dibenz[b,f]oxazepin-11(10H)-ones, via the nucleophilic aromatic substitution (SNAr) of fluorine in 2-fluoro-5-nitrobenzoic acid with the OH of various 2-aminophenols on solid support
  • synthesis of substituted dibenzazocines on solid support, via SNAr of fluorine in 2-fluoro-5-nitrobenzoic acid with the OH function of the immobilized polysubstituted phenols
  • in the synthesis of oxazepines
[Uses]

2-Fluoro-5-nitrobenzoic acid may be used in the synthesis of dibenz[b,f]oxazepin-11(10H)-ones, via the nucleophilic aromatic substitution (SNAr) of fluorine in 2-fluoro-5-nitrobenzoic acid with the OH of various 2-aminophenols on solid support, synthesis of substituted dibenzazocines on solid support, via SNAr of fluorine in 2-fluoro-5-nitrobenzoic acid with the OH function of the immobilized polysubstituted phenols, in the synthesis of oxazepines.
[General Description]

2-Fluoro-5-nitrobenzoic acid is reported to react with an aldehyde, isonitrile and a primary amine tethered to a Boc-protected internal amino or hydroxyl nucleophile, to afford the Ugi product.
[Synthesis]

2-Fluorobenzoic acid

445-29-4

2-Fluoro-5-nitrobenzoic acid

7304-32-7

General procedure for the synthesis of 2-fluoro-5-nitrobenzoic acid from o-fluorobenzoic acid: Nitric acid (60% solution, 5.0 mL) was slowly added dropwise to pre-cooled concentrated sulfuric acid (5.0 mL), and the reaction temperature was controlled to not exceed 10 °C. Subsequently, o-fluorobenzoic acid (2.1 g, 15.0 mmol) was added in batches and the reaction temperature was maintained between 15 and 25 °C. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the reaction was quenched by addition of ice water and the precipitate was collected by filtration. The product was dried at room temperature to give the intermediate 2-fluoro-5-nitrobenzoic acid as a white powder. Yield: 93%; Melting point: 135-137 °C; 1H NMR (300 MHz, DMSO-d6): δ=7.32 (t, 1H, H3, 3JH3_H4=JH3-F=9.2 Hz), 8.43 (dt, 1H, H4, 3JH4_H3=9.2 Hz, 4JH4_F=4JH4_H6=3.5 Hz), 8.89 (dd, 1H, H6, 4JH6_F=5.8 Hz, 4JH6_H4=3.0 Hz); 13C NMR (75 MHz, DMSO-d6): δ=118.7 (d, C1, 2JC-F=10.9 Hz), 118.7 (d, C3, 2JC-F=25.0 Hz), 128.9 (d, C6, 3JC -F=2.2 Hz), 130.6 (d, C4, 3JC-F=10.9 Hz), 143.9 (C5), 165.7 (d, C2, 1JC-F=272.0 Hz), 166.7 (d, COOH, 3JC-F=3.8 Hz).

[References]

[1] Patent: WO2012/85003, 2012, A1. Location in patent: Page/Page column 83
[2] Journal of Organic Chemistry, 2008, vol. 73, # 2, p. 538 - 549
[3] Journal of Heterocyclic Chemistry, 1998, vol. 35, # 6, p. 1301 - 1304
[4] Journal of Medicinal Chemistry, 2003, vol. 46, # 10, p. 1905 - 1917
[5] Australian Journal of Chemistry, 1981, vol. 34, # 5, p. 969 - 979
Spectrum DetailBack Directory
[Spectrum Detail]

2-Fluoro-5-nitrobenzoic acid(7304-32-7)MS
2-Fluoro-5-nitrobenzoic acid(7304-32-7)1HNMR
2-Fluoro-5-nitrobenzoic acid(7304-32-7)13CNMR
2-Fluoro-5-nitrobenzoic acid(7304-32-7)IR1
2-Fluoro-5-nitrobenzoic acid(7304-32-7)IR2
2-Fluoro-5-nitrobenzoic acid(7304-32-7)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Fluoro-5-nitrobenzoic acid, 98%(7304-32-7)
[Alfa Aesar]

2-Fluoro-5-nitrobenzoic acid, 98%(7304-32-7)
[Sigma Aldrich]

7304-32-7(sigmaaldrich)
[TCI AMERICA]

2-Fluoro-5-nitrobenzoic Acid,>98.0%(GC)(T)(7304-32-7)
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