Methyl 4-bromo-2-chloro-6-fluorobenzoate
Methyl 4-bromo-2-chloro-6-fluorobenzoate Basic information
- Product Name:
- Methyl 4-bromo-2-chloro-6-fluorobenzoate
- Synonyms:
-
- Methyl 4-bromo-2-chloro-6-fluorobenzoate
- 4-bromo-2-chloro-6-fluorobenzoic acid methyl ester
- Benzoic acid, 4-bromo-2-chloro-6-fluoro-, methyl ester
- Methyl 4-bromo-6-chloro-2-fluorobenzoate
- CAS:
- 1321613-02-8
- MF:
- C8H5BrClFO2
- MW:
- 267.48
- Mol File:
- 1321613-02-8.mol
Methyl 4-bromo-2-chloro-6-fluorobenzoate Chemical Properties
- Boiling point:
- 299.4±40.0 °C(Predicted)
- Density
- 1.675±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- Appearance
- Colorless to light yellow Liquid
Methyl 4-bromo-2-chloro-6-fluorobenzoate Usage And Synthesis
Synthesis
1321613-01-7
74-88-4
1321613-02-8
Procedure for the synthesis of methyl 4-bromo-2-chloro-6-fluorobenzoate: to a mixture of compound 4-bromo-2-chloro-6-fluorobenzoic acid (20 g, 80 mmol) and potassium carbonate (13.2 g, 96 mmol) in N,N-dimethylformamide (200 mL) was added methylene iodide (23 g, 160 mmol). The reaction mixture was stirred at room temperature for 2 hours and subsequently poured into water (600 mL) and extracted with dichloromethane (2 x 200 mL). The organic layers were combined, washed sequentially with water and brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a brown oil. Purification by silica gel column chromatography (petroleum ether: ethyl acetate = 100:1) gave the target product methyl 4-bromo-2-chloro-6-fluorobenzoate (8 g, 49% yield, two-step reaction) as a light yellow oil.
References
[1] Patent: US2012/28952, 2012, A1. Location in patent: Page/Page column 17
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