Methyl 3-methyl-4-nitrobenzoate
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 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
- InChIKey
- IEFONJKJLZFGKQ-UHFFFAOYSA-N
- CAS DataBase Reference
- 24078-21-5(CAS DataBase Reference)
- NIST Chemistry Reference
- M-toluic acid, 4-nitro-, methyl ester(24078-21-5)
MSDS
- Language:English Provider:ALFA
Methyl 3-methyl-4-nitrobenzoate Usage And Synthesis
Chemical Properties
Off-white or light yellow powder
Uses
The 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
67-56-1
3113-71-1
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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