Basic information Safety Supplier Related

4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER

Basic information Safety Supplier Related

4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER Basic information

Product Name:
4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER
Synonyms:
  • 4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER
  • BENZENEACETIC ACID, 4-METHOXY-3-NITRO-, METHYL ESTER
  • Methyl 2-(4-methoxy-3-nitrophenyl)acetate
  • Methyl 2-(4-methoxy-3-nitrophenyl)
  • 2-(4-METHOXY-3-NITRO PHENYL) ACETIC ACID METHYL ETSER
CAS:
34837-88-2
MF:
C10H11NO5
MW:
225.2
Mol File:
34837-88-2.mol
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4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER Chemical Properties

Melting point:
100-102°
Boiling point:
356.8±27.0 °C(Predicted)
Density 
1.264±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
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Safety Information

HazardClass 
IRRITANT
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4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER Usage And Synthesis

Synthesis

61873-93-6

74-88-4

34837-88-2

General procedure for the synthesis of methyl 2-(4-methoxy-3-nitrophenyl)acetate from methyl 2-(4-hydroxy-3-nitrophenyl)acetate and iodomethane: To a solution of methyl 2-(4-hydroxy-3-nitrophenyl)acetate (4.87 g, 23.1 mmol) was added K2CO3 (8 g, 58 mmol) at room temperature, followed by slow addition of CH3I ( 6.6 g, 46.5 mmol). The reaction mixture was stirred at room temperature overnight. After the reaction was completed, the mixture was poured into ice water (100 mL) and extracted with CH2Cl2 (3 x 300 mL). The organic layers were combined, washed with brine, dried over Na2SO4, filtered and concentrated to give methyl 2-(4-methoxy-3-nitrophenyl)acetate (5 g, 96% yield) as a yellow solid.LCMS analysis showed an [M + H]+ of 226.0; retention time (Rt) of 1.438 min.

References

[1] Patent: WO2013/19682, 2013, A1. Location in patent: Page/Page column 106; 107

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