Methyl 2-methoxy-6-nitrobenzoate

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Methyl 2-methoxy-6-nitrobenzoate Basic information
Product Name:Methyl 2-methoxy-6-nitrobenzoate
Synonyms:thyl2-Methoxy-6-nitrobenzoate;Benzoic acid, 2-methoxy-6-nitro-, methyl ester;Methyl 2-methoxy-6-nitrobenzoate
CAS:77901-52-1
MF:C9H9NO5
MW:211.17
EINECS:
Product Categories:
Mol File:77901-52-1.mol
Methyl 2-methoxy-6-nitrobenzoate Structure
Methyl 2-methoxy-6-nitrobenzoate Chemical Properties
Melting point 63-65 °C(Solv: ethanol (64-17-5))
Boiling point 326.5±22.0 °C(Predicted)
density 1.294±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
Safety Information
MSDS Information
Methyl 2-methoxy-6-nitrobenzoate Usage And Synthesis
Synthesis
2-Methyl-3-nitroanisole

4837-88-1

tert-Butanol

75-65-0

METHYL 2-METHOXY-6-NITROBENZOATE

77901-52-1

General procedure for the synthesis of methyl 2-methoxy-6-nitrobenzoate from 2-methyl-3-nitroanisole and tert-butanol: Potassium permanganate (KMnO4, 5.7 g, 36 mmol) was added to a suspension of 2-methyl-3-nitroanisole (2.0 g, 12 mmol) in tert-butanol (10 mL) and water (20 mL). The reaction mixture was heated to reflux and kept for 4 hours. After completion of the reaction, the cooled mixture was filtered through diatomaceous earth. The filtrate was acidified with 12N aqueous hydrochloric acid and subsequently extracted twice with ethyl acetate (EtOAc). The organic layers were combined, washed sequentially with water and saturated saline, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure. The resulting residue was treated with excess diazomethane/ether (Et2O) solution to afford the target product methyl 2-methoxy-6-nitrobenzoate (548 mg, 22% yield).

References[1] Patent: US2004/106791, 2004, A1. Location in patent: Page 15
Methyl 2-methoxy-6-nitrobenzoate Preparation Products And Raw materials
Raw materials2-Methyl-3-nitroanisole-->tert-Butanol-->Potassium permanganate
Tag:Methyl 2-methoxy-6-nitrobenzoate(77901-52-1) Related Product Information
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