ChemicalBook--->CAS DataBase List--->2945-08-6

2945-08-6

2945-08-6 Structure

2945-08-6 Structure
IdentificationBack Directory
[Name]

Methylp-nitrophenylacetate
[CAS]

2945-08-6
[Synonyms]

Methyl 2-(4-nitrophenyl)
Methyl 2-(4-nitrophenyl)acetate
4-Nitrophenylacetic acid methyl ester
4-Nitrobenzeneacetic acid methyl ester
(4-Nitrophenyl)acetic acid methyl ester
2-(p-Nitrophenyl)acetic acid methyl ester
Benzeneacetic acid, 4-nitro-, methyl ester
[Molecular Formula]

C9H9NO4
[MDL Number]

MFCD00024802
[MOL File]

2945-08-6.mol
[Molecular Weight]

195.17
Questions And AnswerBack Directory
[Appearance]

a pale orange oil
Chemical PropertiesBack Directory
[Melting point ]

52.4-53.3 °C
[Boiling point ]

308.6±17.0 °C(Predicted)
[density ]

1.266±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl p-nitrophenylacetate(2945-08-6)1HNMR
Methyl p-nitrophenylacetate(2945-08-6)IR1
Methyl p-nitrophenylacetate(2945-08-6)IR2
Hazard InformationBack Directory
[Synthesis]

4-nitrophenylacetic acid(2.00 g, 11 mmol) was added to a clean carousel tube. Dimethyl carbonate (3 mL, 3.21 g, 35.6 mmol) was added, and the reaction was heated at reflux overnight. The brown solution was allowed to cool, and poured in to aqueous sodium bicarbonate (10%, 10 mL) while stirring. The resulting mixture was extracted with ethyl acetate (3 x 10 mL). The combined organic layers were washed with water and brine (10 mL each), and dried over anhydrous magnesium sulphate. After filtration and evaporation of the solvents, proton NMR analysis showed the product had formed, and none of the precursor acid remained. No further purification was performed. This gave methyl p-nitrophenylacetate as a pale orange oil (1.929 g, 9.89 mmol, 90%)): 1H NMR (400 MHz, CDCl 3 ) |? 8.20 (d, J = 8.6 Hz, 2H), 7.46 (d, J = 8.6 Hz, 2H, 3.74 (s, 2H), 3.73 (s, 3H).
Synthesis_2945-08-6
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