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Ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate

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Ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate manufacturers

Ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate Basic information
Product Name:Ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate
Synonyms:8-BROMO-4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER;Ux00004205;8-Bromo-4-hydroxy-3-quinolinecarboxylic acid ethyl ester;Ethyl 4-hydroxy-8-broMoquinoline-3-carboxylate;4-Hydroxy-8-broMoquinoline-3-carboxylic acid ethyl ester;ETHYL 8-BROMO-4-HYDROXY-3-QUINOLINECARBOXYLATE;BUTTPARK 89\01-99;3-Quinolinecarboxylic acid, 8-bromo-4-hydroxy-, ethyl ester
CAS:35975-57-6
MF:C12H10BrNO3
MW:296.12
EINECS:
Product Categories:blocks;Bromides;Carboxes;Quinolines
Mol File:35975-57-6.mol
Ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate Structure
Ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate Chemical Properties
Boiling point 385.5±37.0 °C(Predicted)
density 1.593±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka2.16±0.50(Predicted)
form solid
AppearanceOff-white to light brown Solid
InChIInChI=1S/C12H10BrNO3/c1-2-17-12(16)8-6-14-10-7(11(8)15)4-3-5-9(10)13/h3-6H,2H2,1H3,(H,14,15)
InChIKeyXDDQBYKFJZYKPE-UHFFFAOYSA-N
SMILESN1C2C(=CC=CC=2Br)C(O)=C(C(OCC)=O)C=1
Safety Information
Hazard Codes Xi
WGK Germany 3
HS Code 2933499090
Storage Class11 - Combustible Solids
MSDS Information
Ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate Usage And Synthesis
Synthesis
Diethyl ethoxymethylenemalonate

87-13-8

2-Bromoaniline

615-36-1

ETHYL 8-BROMO-4-HYDROXYQUINOLINE-3-CARBOXYLATE

35975-57-6

The reaction was carried out with 2-bromoaniline (2.5 g, 14.62 mmol) and diethyl ethoxymethylene malonate (3.16 g, 14.62 mmol) by heating at 100 °C for 3 hours. Subsequently, the volatiles in the reaction system were removed by a stream of nitrogen. The resulting melt was slowly added to boiling diphenyl ether (10 mL) and the mixture was heated to reflux for 2 hours. After completion of the reaction, the reaction mixture was allowed to cool to room temperature and petroleum ether was added to precipitate the product. The precipitated solid was collected by filtration and dried to give ethyl 4-hydroxy-8-bromoquinoline-3-carboxylate (3.5 g). The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 11.65 (br s, 1H), 8.45 (s, 1H), 8.17 (d, J = 7.8 Hz, 1H), 8.05 (d, J = 7.8 Hz, 1H), 7.39-7.34 (t, J = 7.8 Hz, 1H), 4.26-4.19 (q, J = 7.2,14.1Hz, 2H), 1.30-1.26 (t, J = 6.9Hz, 3H).

References[1] Journal of Organic Chemistry, 2017, vol. 82, # 24, p. 13756 - 13767
[2] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 8, p. 1487 - 1490
[3] Patent: US2003/144507, 2003, A1
[4] Patent: EP1258252, 2002, A1
[5] Patent: US2004/18192, 2004, A1
Ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate Preparation Products And Raw materials
Raw materialsDiethyl ethoxymethylenemalonate-->diethyl {[(2-bromophenyl)amino]methylidene}propanedioate-->2-Bromoaniline
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