3-BroMo-5-(trifluoroMethyl)anisole

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3-BroMo-5-(trifluoroMethyl)anisole Basic information
Product Name:3-BroMo-5-(trifluoroMethyl)anisole
Synonyms:3-BroMo-5-(trifluoroMethyl)anisole;1-Bromo-3-methoxy-5-trifluoromethylbenzene;3-Bromo-5-methoxybenzotrifluoride;Benzene, 1-bromo-3-methoxy-5-(trifluoromethyl)-
CAS:627527-23-5
MF:C8H6BrF3O
MW:255.03
EINECS:
Product Categories:
Mol File:627527-23-5.mol
3-BroMo-5-(trifluoroMethyl)anisole Structure
3-BroMo-5-(trifluoroMethyl)anisole Chemical Properties
Boiling point 201℃
density 1.563
Fp 93℃
storage temp. Sealed in dry,Room Temperature
AppearanceColorless to light yellow Liquid
Safety Information
HS Code 2909309090
MSDS Information
3-BroMo-5-(trifluoroMethyl)anisole Usage And Synthesis
Chemical Propertieslight yellow liquid
Synthesis
3-Methoxy-5-(trifluoromethyl)aniline

349-55-3

3-BroMo-5-(trifluoroMethyl)anisole

627527-23-5

1. 3-Methoxy-5-trifluoromethylaniline (20 g, 104.6 mmol) was added batchwise to a cooled solution of sodium nitrite (7.392 g, 107.1 mmol) in sulfuric acid (74 ml) and acetic acid (88 ml). 2. The mixture was added dropwise to a vigorously stirred solution of cuprous bromide (18 g, 62.8 mmol) in 48% hydrobromic acid (200 ml) at 0°C. 3. The reaction mixture was stirred for 45 minutes at room temperature. 4. The reaction mixture was poured into ice water and the aqueous phase was extracted with dichloromethane. 5. The organic layer was separated. (200 ml) solution. 3. The reaction mixture was stirred at room temperature for 45 min. 4. The reaction mixture was poured into ice water and the aqueous phase was extracted with dichloromethane. 5. The organic layer was separated, dried with anhydrous magnesium sulfate, filtered and the solvent was evaporated at low temperature. 6. The residue was stirred in sodium bicarbonate solution and extracted with diisopropyl ether. 7. The organic layer was separated, dried with anhydrous magnesium sulfate, filtered and the solvent was evaporated to obtain intermediate 3-bromo-5-bromo-5-hydroxybromide. 8. The intermediate 3-bromo-5-trifluoromethyl anisole was obtained (12.7 g, 48% yield).

References[1] Patent: WO2011/33018, 2011, A1. Location in patent: Page/Page column 38
[2] Patent: US2012/172354, 2012, A1. Location in patent: Page/Page column 17
3-BroMo-5-(trifluoroMethyl)anisole Preparation Products And Raw materials
Raw materials3-Bromo-5-trifluoromethylphenol-->3-Methoxy-5-(trifluoromethyl)aniline-->Iodomethane-->Cuprous bromide-->Acetic acid-->Hydrogen bromide-->Sodium nitrite-->Sulfuric acid
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