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