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Methyl 5-methoxy-2-nitrobenzoate

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Methyl 5-methoxy-2-nitrobenzoate Basic information

Product Name:
Methyl 5-methoxy-2-nitrobenzoate
Synonyms:
  • Benzoic acid,5-Methoxy-2-nitro-, Methyl ester
  • 5-Methoxy-2-nitroMethylbenzoate
  • 5-Methoxy-2-nitro-benzoic acid methyl ester
  • Methyl5-methoxy-2-nitrobenzoate98%
  • METHYL 5-METHOXY-2-NITROBENZOATE
  • Methyl 5-methoxy-2-nitrobenzoate 98%
CAS:
2327-45-9
MF:
C9H9NO5
MW:
211.17
Product Categories:
  • Acids & Esters
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Nitro Compounds
  • blocks
  • Carboxes
  • NitroCompounds
  • Aromatic Esters
Mol File:
2327-45-9.mol
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Methyl 5-methoxy-2-nitrobenzoate Chemical Properties

Melting point:
58-59 °C
Boiling point:
196-198 °C(Press: 15-16 Torr)
Density 
1.294±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
crystals
color 
Light lemon/yellow, granular
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2918300090
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Methyl 5-methoxy-2-nitrobenzoate Usage And Synthesis

Description

Methyl 5-methoxy-2-nitrobenzoate is an important organic intermediate, commonly used in organic synthesis. This compound can be synthesized from 5-Hydroxy-2-nitrobenzoic acid.

Synthesis

67-56-1

1882-69-5

2327-45-9

To a pressure-resistant reaction flask was added 5-methoxy-2-nitrobenzoic acid (3.98 g, 20.0 mmol) and anhydrous methanol (10 mL). Concentrated sulfuric acid (150 μL) was added slowly and dropwise. The reaction vial was sealed and the reaction was stirred at 85 °C for 4 days. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to half the original volume. Ethyl acetate (25 mL) was added to dilute, and the organic phase was washed sequentially with water (25 mL), saturated aqueous sodium bicarbonate solution (2 × 25 mL), saturated saline (2 × 25 mL) and water (2 × 25 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford methyl 5-methoxy-2-nitrobenzoate as a yellow oil (3.57 g, 87% yield). Its nuclear magnetic resonance hydrogen spectrum (1H NMR, 300 MHz, CDCl3) data were as follows: δ 8.04 (d, J = 8.8 Hz, 1H, H-6), 7.04 (d, J = 2.3 Hz, 1H, H-3), 7.00 (dd, J = 8.8, 2.8 Hz, 1H, H-4), 3.93 (s, 3H, OCH3), 3.91 (s. 3H, OCH3). The nuclear magnetic resonance carbon spectrum (13C NMR, 75 MHz, CDCl3) data were as follows: δ 166.7, 163.5, 140.2, 131.4, 126.8, 115.9, 114.2, 56.4, 53.5. The obtained data are in agreement with the literature reports.

References

[1] Synlett, 2016, vol. 27, # 8, p. 1237 - 1240
[2] Patent: WO2005/121152, 2005, A1. Location in patent: Page/Page column 30

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