Ethyl 4-bromobenzoylformate

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Products Intro: Product Name:Ethyl 4-bromobenzoyl formate
CAS:20201-26-7
Purity:98%(MinHPLC ) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:ethyl 4-bromobenzoylformate
CAS:20201-26-7
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Products Intro: Product Name:ethyl 2-(4-bromophenyl)-2-oxoacetate
CAS:20201-26-7
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Products Intro: Product Name:Ethyl 2-(4-Bromophenyl)-2-Oxoacetate
CAS:20201-26-7
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Products Intro: Product Name:ETHYL 4-BROMOBENZOYLFORMATE
CAS:20201-26-7
Purity:0.99 Package:5KG;1KG
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
EINECS:
Product Categories:
Mol File:20201-26-7.mol
Ethyl 4-bromobenzoylformate Structure
Ethyl 4-bromobenzoylformate Chemical Properties
Boiling point 322°C
density 1.480
Fp 149°C
storage temp. Sealed in dry,Room Temperature
AppearanceLight yellow to yellow Liquid
Safety Information
Hazard Codes Xi
HS Code 2918999090
MSDS Information
Ethyl 4-bromobenzoylformate Usage And Synthesis
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
Ethyl 4-bromobenzoylformate Preparation Products And Raw materials
Raw materialsEthanol-->Bromobenzene-->Ethyl chlorooxoacetate-->4-Bromobenzoylacetonitrile-->Ethanone, 1-(4-bromophenyl)-2-nitro--->Dichloromethane-->Aluminum chloride
Preparation ProductsEthyl 2-(4-bromophenyl)-2-diazoacetate
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