ChemicalBook--->CAS DataBase List--->690260-94-7

690260-94-7

690260-94-7 Structure

690260-94-7 Structure
IdentificationBack Directory
[Name]

Ethyl 3-bromo-5-nitrobenzoate
[CAS]

690260-94-7
[Synonyms]

Ethyl 3-bromo-5-nitrobenzoate
Ethyl3-bromo-5-nitrobenzoate98%
Ethyl 3-bromo-5-nitrobenzoate 98%
Benzoic acid, 3-bromo-5-nitro-, ethyl ester
Ethyl 3-bromo-5-nitrobenzoate ISO 9001:2015 REACH
[Molecular Formula]

C9H8BrNO4
[MDL Number]

MFCD09258760
[MOL File]

690260-94-7.mol
[Molecular Weight]

274.07
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[color ]

Yellow
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 3-bromo-5-nitrobenzoate(690260-94-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethanol

64-17-5

3-Bromo-5-nitrobenzoic acid

6307-83-1

Ethyl 3-bromo-5-nitrobenzoate

690260-94-7

Add 3-bromo-5-nitrobenzoic acid (25 g, 101.6 mmol) and anhydrous ethanol (200 mL) to a 500 mL round bottom flask. With stirring at 0 °C, sulfoxide chloride (15 mL) was added slowly and dropwise. The reaction mixture was warmed to 80 °C with continuous stirring for 4 hours. Upon completion of the reaction, the reaction was quenched by the addition of 50 mL of water. The reaction mixture was extracted with dichloromethane (3 x 50 mL), the organic layers were combined and concentrated under reduced pressure. The concentrated residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether as eluent (gradient elution, 1:20 to 1:10). Ethyl 3-bromo-5-nitrobenzoate 27.5 g (99% yield) was obtained as a white solid.

[References]

[1] Patent: WO2017/184623, 2017, A1. Location in patent: Page/Page column 127
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 13, p. 3992 - 3996
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