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20201-26-7

20201-26-7 Structure

20201-26-7 Structure
IdentificationBack Directory
[Name]

Ethyl 4-bromobenzoylformate
[CAS]

20201-26-7
[Synonyms]

ETHYL 4-BROMOBENZOYL FORMATE
Ethyl p-bromophenylglyoxylate
ETHYL 4-BROMOPHENYLGLYOXYLATE
2-(4-bromophenyl)-2-oxoacetate
ETHYL 4-(BROMOPHENYL)GLYOXALATE
4-BROMOBENZOYLFORMICACIDETHYLESTER
Ethyl 2-(4-bromophenyl)-2-oxoacetate
Benzeneacetic acid, 4-broMo-α-oxo-, ethyl ester
BENZENEACETIC ACID, 4-BROMO-A-OXO-, ETHYL ESTER
Benzeneacetic acid, 4-bromo-α-oxo-, ethyl ester
[Molecular Formula]

C10H9BrO3
[MDL Number]

MFCD06659764
[MOL File]

20201-26-7.mol
[Molecular Weight]

257.08
Chemical PropertiesBack Directory
[Boiling point ]

322°C
[density ]

1.480
[Fp ]

149°C
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Light yellow to yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xi
[HS Code ]

2918999090
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 4-bromobenzoylformate(20201-26-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Bromobenzene

108-86-1

Ethyl chlorooxoacetate

4755-77-5

Ethyl 4-bromobenzoylformate

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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