ChemicalBook--->CAS DataBase List--->157893-14-6

157893-14-6

157893-14-6 Structure

157893-14-6 Structure
IdentificationBack Directory
[Name]

3-BROMO-5-METHOXYBENZOIC ACID
[CAS]

157893-14-6
[Synonyms]

3-Bromo-5-carboxyanisole
5-BROMO-3-METHOXYBENZOIC ACID
3-BROMO-5-METHOXYBENZOIC ACID
Benzoic acid, 3-bromo-5-methoxy-
3-Bromo-5-methoxybenzoic acid 99%
3-Bromo-5-carboxyanisole, 5-Bromo-m-anisic acid
[Molecular Formula]

C8H7BrO3
[MDL Number]

MFCD00266858
[MOL File]

157893-14-6.mol
[Molecular Weight]

231.04
Chemical PropertiesBack Directory
[Melting point ]

190-191 °C(Solv: ethanol (64-17-5))
[Boiling point ]

338.8±27.0 °C(Predicted)
[density ]

1.625±0.06 g/cm3(Predicted)
[storage temp. ]

Room temperature.
[form ]

powder
[pka]

3.69±0.10(Predicted)
[color ]

White to off-white
[CAS DataBase Reference]

157893-14-6
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
[HS Code ]

2918999090
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMO-5-METHOXYBENZOIC ACID(157893-14-6)1HNMR
3-BROMO-5-METHOXYBENZOIC ACID(157893-14-6)FT-IR
Hazard InformationBack Directory
[Synthesis]

2-AMINO-5-BROMO-3-METHOXYBENZOIC ACID

864293-44-7

3-BROMO-5-METHOXYBENZOIC ACID

157893-14-6

The general procedure for the synthesis of 3-bromo-5-methoxybenzoic acid from 2-amino-5-bromo-3-methoxybenzoic acid was as follows: 2-amino-5-bromo-3-methoxybenzoic acid (4 g, 16.3 mmol) was dissolved in water (20 mL) at 0 °C. Subsequently, concentrated hydrochloric acid (7.5 mL, 90 mmol) and tetrahydrofuran (20 mL) were added to this solution. The reaction mixture was stirred for 30 minutes and then sodium nitrite (3.16 g, 45.8 mmol) was added. After continued stirring for 2 h, hypophosphorous acid (5.1 g, 76 mmol, 50% aqueous solution) was added to the reaction system. The mixture was stirred at room temperature for 16 hours. Upon completion of the reaction, the precipitate was collected by filtration, washed with water and dried under vacuum to afford the target product 3-bromo-5-methoxybenzoic acid (3.2 g, 85% yield). The product was analyzed by ESI-MS, m/z: 229.2 [M-H]?

[References]

[1] Patent: US2009/203677, 2009, A1. Location in patent: Page/Page column 53
[2] Patent: US2009/197871, 2009, A1. Location in patent: Page/Page column 53
[3] Patent: WO2009/100169, 2009, A1. Location in patent: Page/Page column 131
[4] Patent: US2014/288045, 2014, A1. Location in patent: Paragraph 0512
[5] Patent: WO2016/44772, 2016, A1. Location in patent: Paragraph 303; 304
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