Basic information Safety Supplier Related

Ethyl 4-bromobenzoylformate

Basic information Safety Supplier Related

Ethyl 4-bromobenzoylformate Basic information

Product Name:
Ethyl 4-bromobenzoylformate
Synonyms:
  • BENZENEACETIC ACID, 4-BROMO-A-OXO-, ETHYL ESTER
  • Ethyl p-bromophenylglyoxylate
  • ETHYL 4-(BROMOPHENYL)GLYOXALATE
  • ETHYL 4-BROMOPHENYLGLYOXYLATE
  • ETHYL 4-BROMOBENZOYL FORMATE
  • Ethyl 2-(4-bromophenyl)-2-oxoacetate
  • 4-BROMOBENZOYLFORMICACIDETHYLESTER
  • 2-(4-bromophenyl)-2-oxoacetate
CAS:
20201-26-7
MF:
C10H9BrO3
MW:
257.08
Mol File:
20201-26-7.mol
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Ethyl 4-bromobenzoylformate Chemical Properties

Boiling point:
322°C
Density 
1.480
Flash point:
149°C
storage temp. 
Sealed in dry,Room Temperature
Appearance
Light yellow to yellow Liquid
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Safety Information

Hazard Codes 
Xi
HS Code 
2918999090
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Ethyl 4-bromobenzoylformate Usage And Synthesis

Synthesis

108-86-1

4755-77-5

20201-26-7

To a stirred mixture of bromobenzene (0.7 mL, 6.5 mmol) and monoethyl oxalyl chloride (0.7 mL, 6.5 mmol) in dichloromethane (12 mL) was added aluminum trichloride (1.7 g, 12.5 mmol) in one batch. The reaction mixture was stirred at 0°C for 30 minutes before slowly warming to room temperature and continuing to stir for 18 hours. After completion of the reaction, the mixture was carefully poured into concentrated hydrochloric acid at 0°C to quench the reaction. Subsequently, the mixture was extracted with dichloromethane (3 × 100 mL). The organic layers were combined, washed with saturated saline (100 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate/petroleum ether = 1:20) to afford ethyl 4-bromophenylglyoxylate (1.0 g, 60% yield) as a yellow oil. Mass spectrometry (ESI+) analysis: C10H9BrO3 theoretical value [M+H]+ 256, measured value 257, 259 [M+H]+.

References

[1] Journal of Organic Chemistry, 1996, vol. 61, # 18, p. 6407 - 6415
[2] Tetrahedron Letters, 2006, vol. 47, # 16, p. 2675 - 2678
[3] Chemical Science, 2018, vol. 9, # 48, p. 8930 - 8936
[4] Patent: US2016/31892, 2016, A1. Location in patent: Paragraph 0156-0158
[5] Journal of Organic Chemistry, 2008, vol. 73, # 10, p. 3842 - 3847

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