| Identification | More | [Name]
Ethyl 2-bromobenzoate | [CAS]
6091-64-1 | [Synonyms]
2-BROMOBENZOIC ACID ETHYL ESTER
ETHYL 2-BROMOBENZOATE
RARECHEM AL BI 0014
2-Bromobezoic acid, ethyl ester
Ethyl 2-bromobenzoate, 98+% | [EINECS(EC#)]
228-034-3 | [Molecular Formula]
C9H9BrO2 | [MDL Number]
MFCD00015443 | [Molecular Weight]
229.07 | [MOL File]
6091-64-1.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [HS Code ]
29163990 |
| Hazard Information | Back Directory | [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 |
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