3-METHOXY-5-METHYL-BENZOIC ACID METHYL ESTER
3-METHOXY-5-METHYL-BENZOIC ACID METHYL ESTER Basic information
- Product Name:
- 3-METHOXY-5-METHYL-BENZOIC ACID METHYL ESTER
- Synonyms:
-
- 3-METHOXY-5-METHYL-BENZOIC ACID METHYL ESTER
- Methyl 3-Methoxy-5-Methylbenzoate
- Benzoic acid, 3-Methoxy-5-Methyl-, Methyl ester
- Methyl 3-methyl-5-(methyloxy)benzoate
- Methyl 5-methoxy-3-methylbenzoate
- CAS:
- 108593-44-8
- MF:
- C10H12O3
- MW:
- 180.2
- Mol File:
- 108593-44-8.mol
3-METHOXY-5-METHYL-BENZOIC ACID METHYL ESTER Chemical Properties
- Boiling point:
- 270.8±20.0 °C(Predicted)
- Density
- 1.075±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- Colorless to light yellow Liquid
3-METHOXY-5-METHYL-BENZOIC ACID METHYL ESTER Usage And Synthesis
Synthesis
2615-71-6
74-88-4
108593-44-8
General procedure for the synthesis of methyl 3-methoxy-5-methylbenzoate from methyl 3-hydroxy-5-methylbenzoate and iodomethane: To a solution of methyl 3-hydroxy-5-methylbenzoate (20.0 g, 120 mmol) in N,N-dimethylformamide (120 mL) was added sequentially iodomethane (11.2 mL, 180 mmol), cesium carbonate (4.65 g, 180 mmol) and catalytic amount of 4-dimethylaminopyridine. 180 mmol) and a catalytic amount of 4-dimethylaminopyridine. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, it was diluted with water (200 mL) and extracted with ethyl acetate (3 x 150 mL). The organic phases were combined, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated to afford the target product methyl 3-methoxy-5-methylbenzoate (19.9 g, 92% yield). The product was characterized by 1H NMR (400 MHz, CDCl3): δ 2.38 (s, 3H), 3.84 (s, 3H), 3.91 (s, 3H), 6.93 (s, 1H), 7.37 (s, 1H), 7.48 (s, 1H).
References
[1] Patent: WO2007/105058, 2007, A2. Location in patent: Page/Page column 49
[2] Patent: WO2009/32667, 2009, A1. Location in patent: Page/Page column 137
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