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888327-32-0

888327-32-0 Structure

888327-32-0 Structure
IdentificationBack Directory
[Name]

4-Bromo-1-difluoromethoxy-2-methyl-benzene
[CAS]

888327-32-0
[Synonyms]

5-Bromo-2-(difluoromethoxy)toluene
4-BroMo-2-Methy-1-(difluoroMethoxy)benzene
4-Bromo-1-difluoromethoxy-2-methyl-benzene
1-Bromo-3-methyl-4-(difluoromethoxy)benzene
Benzene, 4-bromo-1-(difluoromethoxy)-2-methyl-
[Molecular Formula]

C8H7BrF2O
[MDL Number]

MFCD11036069
[MOL File]

888327-32-0.mol
[Molecular Weight]

237.04
Chemical PropertiesBack Directory
[Boiling point ]

223℃
[density ]

1.508
[Fp ]

108℃
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

liquid
[color ]

Colourless
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[HS Code ]

2909309090
Spectrum DetailBack Directory
[Spectrum Detail]

4-Bromo-1-difluoromethoxy-2-methyl-benzene(888327-32-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzenamine, 4-(difluoromethoxy)-3-methyl-

83190-02-7

4-Bromo-1-difluoromethoxy-2-methyl-benzene

888327-32-0

General procedure for the synthesis of 5-bromo-2-(difluoromethoxy)toluene from 4-(difluoromethoxy)-3-methylaniline: to a stirred solution of 4-amino-1-(difluoromethoxy)-2-methylbenzene (5 g, 28.90 mmol) in a mixture of hydrobromic acid (20 mL) and water (20 mL), at 0 °C, sodium nitrite (2.07 g 30.00 mmol) in aqueous solution (10 mL), and the titration process was controlled to be completed within 20 minutes. After the dropwise addition, the reaction mixture was continued to be stirred at 0 °C for 30 min. Subsequently, copper (I) bromide (4 g, 27.87 mmol) was added and the mixture was heated to 60 °C for 30 min of reaction. Upon completion of the reaction, the reaction mixture was extracted with ethyl acetate (3 x 50 mL), the organic layers were combined, washed once with water (10 mL), dried over anhydrous sodium sulfate and concentrated to give 2.5 g of 4-bromo-1-(difluoromethoxy)-2-methylbenzene in 37% yield.

[References]

[1] Patent: WO2006/55187, 2006, A1. Location in patent: Page/Page column 83
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