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Methyl 3-methyl-4-nitrobenzoate

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Methyl 3-methyl-4-nitrobenzoate Basic information
Product Name:Methyl 3-methyl-4-nitrobenzoate
Synonyms:Methyl 3-Methyl-4-nitrobenzoate , 98.0%(GC);4-NITRO-M-TOLUIC ACID METHYL ESTER;BENZOIC ACID, 3-METHYL-4-NITRO-METHYL ESTER;BUTTPARK 62\04-20;METHYL 3-METHYL-4-NITROBENZENECARBOXYLATE;METHYL 3-METHYL-4-NITROBENZOATE;3-METHYL-4-NITROBENZOIC ACID METHYL ESTER;3-methyl-4-nitro benzoate
CAS:24078-21-5
MF:C9H9NO4
MW:195.17
EINECS:230-886-6
Product Categories:FINE Chemical & INTERMEDIATES;Benzoic acid;Esters;Phenyls & Phenyl-Het;pharmaceutical intermediates;blocks;Carboxes;NitroCompounds;Aromatic Esters
Mol File:24078-21-5.mol
Methyl 3-methyl-4-nitrobenzoate Structure
Methyl 3-methyl-4-nitrobenzoate Chemical Properties
Melting point 80 °C
Boiling point 318.5±30.0 °C(Predicted)
density 1+-.0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
color White to Yellow
InChIKeyIEFONJKJLZFGKQ-UHFFFAOYSA-N
CAS DataBase Reference24078-21-5(CAS DataBase Reference)
NIST Chemistry ReferenceM-toluic acid, 4-nitro-, methyl ester(24078-21-5)
Safety Information
Hazard Codes Xi
Risk Statements 20/21/22
Safety Statements 24/25
HS Code 2916399090
MSDS Information
ProviderLanguage
ALFA English
Methyl 3-methyl-4-nitrobenzoate Usage And Synthesis
Chemical PropertiesOff-white or light yellow powder
UsesThe presence of the nitro group contributes to its potential reactivity and polar nature, while the methyl ester group enhances its solubility in organic solvents. Methyl 3-methyl-4-nitrobenzoate is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals.
Synthesis
Methanol

67-56-1

3-Methyl-4-nitrobenzoic acid

3113-71-1

Methyl 3-methyl-4-nitrobenzoate

24078-21-5

Step 1. Synthesis of methyl 3-methyl-4-nitrobenzoate 3-Methyl-4-nitrobenzoic acid (30 g, 165.61 mmol) was dissolved in methanol (300 mL), stirred at 0°C and thionyl chloride (25 mL) was added slowly and dropwise. The reaction mixture was warmed to 80°C and stirring was continued for 1 hour. Upon completion of the reaction, the mixture was concentrated under reduced pressure to give the crude product. The crude product was dissolved in petroleum ether (100 mL) and filtered to give methyl 3-methyl-4-nitrobenzoate as a white solid (31 g, 96% yield). Product Characterization: LC/MS (ES, m/z): [M + H]+ 196.01 1H-NMR (300MHz, CD3Cl) δ 7.99-8.04 (m, 3H), 3.98 (s, 3H), 2.64 (s, 3H)

References[1] Patent: US2012/277224, 2012, A1. Location in patent: Page/Page column 33
[2] Chemical Communications, 2012, vol. 48, # 94, p. 11558 - 11560
[3] Chemical Communications, 2007, # 5, p. 504 - 506
[4] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 14, p. 4582 - 4589
[5] Chemistry - An Asian Journal, 2010, vol. 5, # 7, p. 1573 - 1585
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