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4,5-DIFLUORO-2-NITROBENZOIC ACID METHYL ESTER

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4,5-DIFLUORO-2-NITROBENZOIC ACID METHYL ESTER Basic information

Product Name:
4,5-DIFLUORO-2-NITROBENZOIC ACID METHYL ESTER
Synonyms:
  • 4,5-DIFLUORO-2-NITROBENZOIC ACID METHYL ESTER
  • METHYL 4,5-DIFLUORO-2-NITROBENZOATE
  • methyl 3,4-difluoro-6-nitro benzoate
  • Benzoic acid, 4,5-difluoro-2-nitro-, methyl ester
  • 4,5-DIFLUORO-2-NITROBENZOIC ACID METHYL ESTER ISO 9001:2015 REACH
CAS:
1015433-96-1
MF:
C8H5F2NO4
MW:
217.13
Product Categories:
  • Fluorine series
  • Aromatic Esters
Mol File:
1015433-96-1.mol
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4,5-DIFLUORO-2-NITROBENZOIC ACID METHYL ESTER Chemical Properties

Melting point:
59-63°
Boiling point:
288℃
Density 
1.471
Flash point:
128℃
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
InChI
InChI=1S/C8H5F2NO4/c1-15-8(12)4-2-5(9)6(10)3-7(4)11(13)14/h2-3H,1H3
InChIKey
JHWZADUIXGMAKM-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC(F)=C(F)C=C1[N+]([O-])=O
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Safety Information

HS Code 
2916399090
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4,5-DIFLUORO-2-NITROBENZOIC ACID METHYL ESTER Usage And Synthesis

Uses

Methyl 4,5-difluoro-2-nitrobenzoate is mainly used as an intermediate in organic synthesis.

Synthesis

67-56-1

20372-63-8

1015433-96-1

Step 2 (Ib): to a solution of anhydrous methanol (MeOH, 1.0 L) of 4,5-difluoro-2-nitrobenzoic acid (Ia, 40.0 g, 196.947 mmol) was slowly added concentrated sulfuric acid (H2SO4, 60.0 mL), and the reaction mixture immediately became clear. The reaction system was heated to reflux with continuous stirring for 2 days. After completion of the reaction, methanol was removed by rotary evaporator under reduced pressure. The residue was liquefied with ethyl acetate (EtOAc) and water and the organic phase was collected. The organic phase was sequentially washed with saturated brine and dried over anhydrous magnesium sulfate (MgSO4). After filtration, the filtrate was treated with anhydrous sodium sulfate (Na2SO4), filtered again, and the filtrate was concentrated to give methyl 4,5-difluoro-2-nitrobenzoate as a light yellow solid with a yield of 39.71 g and 93% yield.

References

[1] Patent: WO2008/36843, 2008, A2. Location in patent: Page/Page column 33

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