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790230-04-5

790230-04-5 Structure

790230-04-5 Structure
IdentificationBack Directory
[Name]

4-broMo-3-(hydroxyMethyl)benzoic acid
[CAS]

790230-04-5
[Synonyms]

4-broMo-3-(hydroxyMethyl)benzoic acid
Benzoic acid, 3-bromo-4-(bromomethyl)-
[Molecular Formula]

C8H7BrO3
[MDL Number]

MFCD16249537
[MOL File]

790230-04-5.mol
[Molecular Weight]

231.043
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2918199890
Spectrum DetailBack Directory
[Spectrum Detail]

4-broMo-3-(hydroxyMethyl)benzoic acid(790230-04-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

methyl 3-(acetoxymethyl)-4-bromobenzoate

254746-41-3

4-broMo-3-(hydroxyMethyl)benzoic acid

790230-04-5

b) Synthesis of 4-bromo-3-(hydroxymethyl)benzoic acid A solution of lithium hydroxide monohydrate (2.278 g, 54.3 mmol) in water (12 mL) was slowly added to a solution of tetrahydrofuran (40 mL) containing methyl 3-(acetoxymethyl)-4-bromobenzoate (3.89 g), and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the pH was adjusted with 2 M hydrochloric acid solution to about 1. Subsequently, an appropriate amount of water and ethyl acetate were added for extraction, and the aqueous phase was re-extracted with ethyl acetate. All organic phases were combined, washed sequentially with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to afford the title compound 4-bromo-3-(hydroxymethyl)benzoic acid 3.06 g in 98% yield. The product was characterized by 1H NMR (500 MHz, DMSO-d6): δ 13.15 (br.s, 1H), 8.11 (d, 1H), 7.65-7.76 (m, 2H), 5.55-5.69 (m, 1H), 4.54 (d, 2H); mass spectra (ESI) m/z 229,231 [M-1]-.

[References]

[1] Patent: WO2010/132016, 2010, A1. Location in patent: Page/Page column 74
[2] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 23, p. 7688 - 7705
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