Ethyl 2-bromobenzoate Chemical Properties

Boiling point:

117 °C/17 mmHg (lit.)

Density 

1.443 g/mL at 25 °C (lit.)

refractive index 

n20/D 1.544(lit.)

Flash point:

>230 °F

storage temp. 

Sealed in dry,Room Temperature

solubility 

Dichloromethane, Ethyl Acetate

form 

Liquid

color 

Clear yellow

BRN 

2207360

CAS DataBase Reference

6091-64-1(CAS DataBase Reference)

NIST Chemistry Reference

Ethyl 2-bromobenzoate(6091-64-1)

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

37/39-26

WGK Germany 

3

HS Code 

29163990

MSDS

• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Ethyl 2-bromobenzoate Usage And Synthesis

Chemical Properties

clear yellow liquid

Uses

Ethyl 2-bromobenzoate is an intermediate of 7H-Benzo[c]fluorene, which is a polycyclic aomatic hydrocarbon (PAH) with mutagenic activity. 7H-Benzo[c]fluorene is a major DNA adduct-forming component of coal tar. Recent studies suggest that 7H-Benzo[c]fluorene may be capable of inducing lung tumors.

General Description

Ethyl 2-bromobenzoate is an halobenzoic acid ethyl ester. Silylation and hydrolysis of ethyl 2-bromobenzoate has been reported.

Synthesis

O-bromobenzoic acid (5 g, 24.87 mmol) was dissolved in anhydrous ethanol (100 mL). Concentrated sulfuric acid (5 mL) was slowly added as a catalyst, a reflux condensing unit was installed, and the system was heated to reflux temperature in an oil bath with continuous stirring for 24 hours. After the reaction was completed, the reaction system was cooled to room temperature. Most of the ethanol solvent was removed by concentration under reduced pressure by rotary evaporator. The residue was transferred to a partition funnel, washed with deionized water to remove acidic impurities, and subsequently extracted with ethyl acetate (3 x 50 mL). The organic phases were combined and dried with anhydrous magnesium sulfate for 30 min. The desiccant was removed by filtration and the filtrate was concentrated by rotary evaporation to obtain the crude product. Finally, the crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate=10:1) to afford ethyl 2-bromobenzoate (4.9 g, 86% yield) as a colorless oily liquid.

References

[1] Journal of Organic Chemistry, 2007, vol. 72, # 5, p. 1803 - 1806
[2] Patent: CN105555761, 2016, A. Location in patent: Paragraph 0344; 0345; 0346
[3] Patent: US9896467, 2018, B1. Location in patent: Page/Page column 32; 33
[4] Patent: CN108164532, 2018, A. Location in patent: Paragraph 0076; 0078; 0079
[5] Journal of the American Chemical Society, 1944, vol. 66, p. 914,917

Ethyl 2-bromobenzoate(6091-64-1)Related Product Information

• Ethyl cyanoacetate
• Urethane
• Ethylparaben
• 2-Bromofluorobenzene
• Ethyl formate
• ISOXADIFEN-ETHYL
• 2-Bromobenzoic acid
• ETHYL ANTHRANILATE
• Ethanol
• Ethyl acetate
• Trinexapac-ethyl
• Ethyl benzoate
• Triethyl orthoformate
• Ethyl cyanoformate
• Ethyl propiolate
• Ethyl acrylate
• Methyl 2-bromobenzoate
• Benzocaine