ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE

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Products Intro: Product Name:Ethyl 5-bromobenzofuran-2-carboxylate
CAS:84102-69-2
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Products Intro: Product Name:Ethyl 5-bromobenzofuran-2-carboxylate
CAS:84102-69-2
Purity:98%(Min.HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:84102-69-2
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ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE manufacturers

ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE Basic information
Product Name:ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE
Synonyms:ETHYL 5-BROMO-1-BENZOFURAN-2-CARBOXYLATE;ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE;AURORA 22531;Ethyl(5-bromobenzofurane)-2-carboxylate;Ethyl 5-bromobenzo[b]furan-2-carboxylate;2-Benzofurancarboxylic acid, 5-bromo-, ethyl ester;5-Bromo-2-(ethoxycarbonyl)-1-benzofuran;5-broMobenzofuran-2-carboxylate
CAS:84102-69-2
MF:C11H9BrO3
MW:269.09
EINECS:
Product Categories:
Mol File:84102-69-2.mol
ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE Structure
ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE Chemical Properties
Melting point 60-62°
Boiling point 328.3±22.0 °C(Predicted)
density 1.520±0.06 g/cm3(Predicted)
storage temp. 2-8°C
AppearanceWhite to off-white Solid
InChIInChI=1S/C11H9BrO3/c1-2-14-11(13)10-6-7-5-8(12)3-4-9(7)15-10/h3-6H,2H2,1H3
InChIKeyXLJWAHXKBCDQNP-UHFFFAOYSA-N
SMILESO1C2=CC=C(Br)C=C2C=C1C(OCC)=O
CAS DataBase Reference84102-69-2
Safety Information
Hazard Codes Xi
HazardClass IRRITANT
HS Code 2932990090
MSDS Information
ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE Usage And Synthesis
UsesEthyl 5-bromobenzofuran-2-carboxylate
Synthesis
Ethyl bromoacetate

105-36-2

5-Bromosalicylaldehyde

1761-61-1

ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE

84102-69-2

5-Bromosalicylaldehyde (5 g, 25 mmol, 1.0 eq.) and cesium carbonate (8.2 g, 25 mmol, 1.0 eq.) were dissolved in 80 ml of DMF and stirred well. Subsequently, ethyl bromoacetate (8.3 g, 50 mmol, 2.0 eq.) was slowly added to the reaction system. The reaction mixture was stirred at room temperature for 30 min. After that, the reaction temperature was increased to 120 °C for 2 hours. The reaction progress was monitored by TLC. After completion of the reaction, the mixture was cooled to room temperature and poured into ice water and stirred vigorously for 30 minutes. The precipitate was collected by filtration, the filter cake was washed with water and dried to give the yellow powdery solid product ethyl 5-bromobenzofuran-2-carboxylate (4 g, 59.7% yield).

References[1] Patent: CN106478564, 2017, A. Location in patent: Paragraph 0216; 0217; 0218
[2] Patent: CN107383024, 2017, A. Location in patent: Paragraph 0473
[3] Patent: US2004/209865, 2004, A1
[4] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 20, p. 5591 - 5593
Tag:ETHYL(5-BROMOBENZOFURAN)-2-CARBOXYLATE(84102-69-2) Related Product Information
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