ChemicalBook--->CAS DataBase List--->453565-90-7

453565-90-7

453565-90-7 Structure

453565-90-7 Structure
IdentificationBack Directory
[Name]

3-Bromo-5-(trifluoromethoxy)Benzoicacid
[CAS]

453565-90-7
[Synonyms]

Benzoic acid, 3-bromo-5-(trifluoromethoxy)-
3-Bromo-5-(trifluoromethoxy)benzoic acid 97%
3-BROMO-5-(TRIFLUOROMETHOXY)BENZOIC ACID,99.8%
[Molecular Formula]

C8H4BrF3O3
[MDL Number]

MFCD04116041
[MOL File]

453565-90-7.mol
[Molecular Weight]

285.02
Chemical PropertiesBack Directory
[Melting point ]

87-89℃
[Boiling point ]

290.6±40.0 °C(Predicted)
[density ]

1.797±0.06 g/cm3(Predicted)
[storage temp. ]

Room temperature.
[form ]

solid
[pka]

3.43±0.10(Predicted)
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[RIDADR ]

UN2811
[HS Code ]

2918999090
Spectrum DetailBack Directory
[Spectrum Detail]

3-Bromo-5-(trifluoromethoxy)Benzoicacid(453565-90-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzoic acid, 4-amino-3-bromo-5-(trifluoromethoxy)-

453565-89-4

3-Bromo-5-(trifluoromethoxy)Benzoicacid

453565-90-7

4-Amino-3-bromo-5-(trifluoromethoxy)benzoic acid (1.5 g, 5 mmol) was used as starting material, which was mixed with ethanol (15 mL) at 0 °C. Subsequently, concentrated sulfuric acid (2.26 g, 10.2 mmol) was slowly added. An aqueous solution (1.2 mL) of sodium nitrite (0.38 g, 5.5 mmol) was added dropwise at 0 °C and the dropwise process lasted for 1 hour. After the reaction mixture was gradually warmed to room temperature, it was heated to reflux for 45 min. Upon completion of the reaction, the reaction was terminated by the addition of water. The reaction mixture was extracted with dichloromethane and the organic phase was separated. The dichloromethane layer was dried and concentrated to give the crude product. The crude product was dissolved in 1M sodium hydroxide solution and extracted with ether to remove impurities. The aqueous phase was acidified with 2M HCl to pH=2 and precipitated as a solid, which was filtered and dried to give the target product 3-bromo-5-(trifluoromethoxy)benzoic acid (1.08 g, 75.5% yield).

[References]

[1] Patent: US2003/55085, 2003, A1
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