2-Bromo-5-hydroxypyridine Chemical Properties

Melting point:

135.5-136.5°C

Boiling point:

373.0±22.0 °C(Predicted)

Density 

1.788±0.06 g/cm3(Predicted)

storage temp. 

Keep in dark place,Sealed in dry,Room Temperature

form 

powder to crystal

pka

8.69±0.10(Predicted)

color 

White to Almost white

Water Solubility 

Slightly soluble in water.

InChI

InChI=1S/C5H4BrNO/c6-5-2-1-4(8)3-7-5/h1-3,8H

InChIKey

PTEFNEALEPSHLC-UHFFFAOYSA-N

SMILES

C1=NC(Br)=CC=C1O

CAS DataBase Reference

55717-45-8(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xi,Xn

Risk Statements 

22-36/37/38

Safety Statements 

26-37

HazardClass 

IRRITANT

HS Code 

29339900

2-Bromo-5-hydroxypyridine Usage And Synthesis

Chemical Properties

Light yellow Cryst

Uses

It is used as an active pharmaceutical intermediate and in the coupling reactions with halo aromatic amines and alcohols for a practical synthetic route to 2-substituted amino phenyl and hydroxyphenyl pyridines.

Uses

6-Bromo-3-pyridinol is a pyridine derivative that was shown exhibit antioxidant properties.

Synthesis

To a 250 mL three-necked flask equipped with a mechanical stirrer, thermocouple, and nitrogen inlet, 2,5-dibromopyridine (9.98 g, 42.1 mmol) was added to 53 mL of anhydrous THF under a nitrogen atmosphere and dissolved to form a light tan solution. An ether solution (23 mL) of 2 M isopropylmagnesium chloride (i-PrMgCl) was slowly added via syringe over 3 min. The reaction mixture was transformed into a brown suspension when about 50% of Grignard reagent was added. The addition of i-PrMgCl triggered an exothermic reaction and the temperature was raised to 36 °C. After 90 min of continuous stirring, the suspension was cooled to 2 °C and trimethylborate (B(OMe)3) was rapidly added via syringe. The reaction was exothermic to 6 °C, followed by removal of the ice bath. After stirring overnight, glacial acetic acid (3.79 g) was added to dissolve all solids to form a dark brown solution. The solution was cooled in an ice bath and 5.25 g of 30% hydrogen peroxide solution was slowly added dropwise, with the rate of dropwise acceleration controlled to keep the reaction temperature from exceeding 12 °C. The reaction was then heated to 6 °C with stirring overnight. After the dropwise addition, stirring was continued for 90 minutes, followed by the addition of ether (150 mL) and water (100 mL) for extraction. The aqueous layer was separated and further extracted with ether (2 x 100 mL). The organic phases were combined and washed sequentially with 100 mL of 10% sodium bisulfite solution and brine. The organic phase was dried over anhydrous magnesium sulfate (MgSO4) and concentrated by rotary evaporation to a brown oil, which solidified on standing to give a brown solid (7.95 g). The crude product was adsorbed on 15 g Celite and purified by rapid column chromatography using a 220 g silica gel column with hexane/ethyl acetate gradient elution. The target fraction was collected and evaporation of the solvent gave 4.81 g of off-white solid product in 66% yield. The nuclear magnetic resonance (NMR) spectrum of the product was consistent with that of the 6-bromo-3-pyridinol standard.1H NMR (DMSO-d6, 400 MHz) δ 10.24 (s, 1H), 7.94 (d, J = 3.0 Hz, 1H), 7.42 (d, J = 8.6 Hz, 1H), 7.17 (dd, J = 3.0, 8.6 Hz, 1H); 13C NMR (DMSO-d6, 101 MHz) δ 153.74, 138.13, 129.30, 128.14, 126.21.

References

[1] Patent: WO2017/87597, 2017, A1. Location in patent: Page/Page column 4; 5
[2] Patent: WO2017/87619, 2017, A1. Location in patent: Page/Page column 5; 6
[3] Patent: WO2017/87643, 2017, A1. Location in patent: Page/Page column 5; 6
[4] ChemPlusChem, 2017, vol. 82, # 5, p. 758 - 769
[5] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 23, p. 5835 - 5839

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