2-Bromo-3-nitrophenol Chemical Properties

Melting point:

147.5°C

Boiling point:

248°C

Density 

1.881

refractive index 

1.6090 (estimate)

Flash point:

104°C

storage temp. 

under inert gas (nitrogen or Argon) at 2–8 °C

form 

powder

pka

7.39±0.25(Predicted)

color 

Beige/brown

InChI

InChI=1S/C6H4BrNO3/c7-6-4(8(10)11)2-1-3-5(6)9/h1-3,9H

InChIKey

HRVRWIBVVHOHNN-UHFFFAOYSA-N

SMILES

C1(O)=CC=CC([N+]([O-])=O)=C1Br

Safety Information

HS Code 

2908990000

2-Bromo-3-nitrophenol Usage And Synthesis

Synthesis

General procedure for the synthesis of 2-bromo-3-nitrophenol from 2-amino-3-nitrophenol: 2-amino-3-nitrophenol (5 g, 32.4 mmol) was dissolved in water (29.5 mL) and 1,4-dioxane (14.7 mL). The mixture was heated to reflux and hydrobromic acid (48%, 16.7 mL, 147 mmol) was added dropwise over 20 min. After addition, reflux was continued for 15 min. The reaction mixture was cooled to 0 °C (ice bath) and a solution of sodium nitrite (2.23 g, 32.3 mmol) in water (20 mL) was added over 30 min. Stirring was continued at 0 °C for 15 min, then the mixture was transferred to a pre-cooled jacketed dropping funnel (0 °C) and added dropwise to a stirred mixture of cuprous bromide (I) (5.34 g, 37.2 mmol) in water (29.5 mL) and hydrobromic acid (48%, 16.7 mL, 147 mmol). The reaction mixture was stirred at 0 °C for 15 min, then warmed to 60 °C, continued stirring for 15 min, cooled to room temperature, and stirred overnight. The reaction mixture was transferred to a partition funnel and extracted with ether (3 x 150 mL). The organic layers were combined, washed with brine (1 x 150 mL), dried (Na2SO3), filtered and concentrated to give the crude product (7.99 g) as a reddish brown oil. The crude product was extracted by fast column chromatography (1:25 ultrapure silica gel, 230-400 mesh, 40-60 mm, 60 ? ; CH2Cl2 as solvent) purified the crude product to afford pure 2-bromo-3-nitrophenol (45%, 3.16 g) as an orange-brown solid. Mass spectrum (MS) m/z: 217.8 (MH+). High performance liquid chromatography (HPLC, TFA) homogeneity at 220 nm: 97%.

References

[1] Chemistry - A European Journal, 2017, vol. 23, # 42, p. 9996 - 10000
[2] Patent: JP2005/522501, 2005, A. Location in patent: Page/Page column 18
[3] Patent: WO2009/92590, 2009, A2. Location in patent: Page/Page column 69-70
[4] Patent: WO2009/109539, 2009, A2. Location in patent: Page/Page column 65; 66
[5] Patent: WO2004/103996, 2004, A1. Location in patent: Page 40

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