ChemicalBook--->CAS DataBase List--->34837-88-2

34837-88-2

34837-88-2 Structure

34837-88-2 Structure
IdentificationBack Directory
[Name]

4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER
[CAS]

34837-88-2
[Synonyms]

Methyl 2-(4-methoxy-3-nitrophenyl)
Methyl 2-(4-methoxy-3-nitrophenyl)acetate
4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER
BENZENEACETIC ACID, 4-METHOXY-3-NITRO-, METHYL ESTER
[Molecular Formula]

C10H11NO5
[MDL Number]

MFCD09754963
[MOL File]

34837-88-2.mol
[Molecular Weight]

225.2
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H227
[Precautionary statements ]

P501-P210-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313-P403+P235
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER(34837-88-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl  (4-Hydroxy-3-nitrophenyl)acetate

61873-93-6

Iodomethane

74-88-4

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

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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