ChemicalBook--->CAS DataBase List--->933785-18-3

933785-18-3

933785-18-3 Structure

933785-18-3 Structure
IdentificationBack Directory
[Name]

4-Bromo-2-(trifluoromethoxy)benzoic acid methyl ester
[CAS]

933785-18-3
[Synonyms]

2- trifluoromethoxy-4-bromobenzoate
Methyl 4-bromo-2-(trifluoromethoxy)
Ethyl 4-bromo-2-(trifluoromethoxy)benzoate
4-Bromo-2-(trifluoromethoxy)benzoic acid methyl ester
Benzoic acid, 4-bromo-2-(trifluoromethoxy)-, methyl ester
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C9H6BrF3O3
[MDL Number]

MFCD12761592
[MOL File]

933785-18-3.mol
[Molecular Weight]

299.04
Chemical PropertiesBack Directory
[Boiling point ]

266℃
[density ]

1.626
[Fp ]

115℃
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

liquid
[color ]

Clear, colourless
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H227-H315-H319-H335
[Precautionary statements ]

P305+P351+P338
[HS Code ]

2918999090
Spectrum DetailBack Directory
[Spectrum Detail]

4-Bromo-2-(trifluoromethoxy)benzoic acid methyl ester(933785-18-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

4-Bromo-2-(trifluoromethoxy)benzoic acid

509142-48-7

4-Bromo-2-(trifluoromethoxy)benzoic acid methyl ester

933785-18-3

General procedure for the synthesis of methyl 4-bromo-2-(trifluoromethoxy)benzoate from methanol and 4-bromo-2-trifluoromethoxybenzoic acid: the compound 4-bromo-2-trifluoromethoxybenzoic acid (30.0 g, 0.11 mol) was suspended in a 4 M methanol-hydrochloric acid solution (500 mL), and the reaction was carried out at reflux overnight. After completion of the reaction, methanol was removed by distillation under reduced pressure. The resulting residue was extracted by partitioning with saturated sodium carbonate solution and ethyl acetate. The organic layer was dried with anhydrous sodium sulfate and concentrated under reduced pressure to afford the target product methyl 4-bromo-2-(trifluoromethoxy)benzoate (24.0 g, 77% yield).

[References]

[1] Patent: US2012/28952, 2012, A1. Location in patent: Page/Page column 19
[2] Journal of Medicinal Chemistry, 2010, vol. 53, # 16, p. 5979 - 6002
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