6-CHLORO-4-HYDROXYQUINOLINE

6-CHLORO-4-HYDROXYQUINOLINE Suppliers list
Company Name: TCI (Shanghai) Development Co., Ltd.  
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6-CHLORO-4-HYDROXYQUINOLINE manufacturers

6-CHLORO-4-HYDROXYQUINOLINE Basic information
Product Name:6-CHLORO-4-HYDROXYQUINOLINE
Synonyms:4-HYDROXY-6-CHLOROQUINOLINE;6-CHLORO-4-HYDROXYQUINOLINE;6-CHLOROQUINOLIN-4(1H)-ONE;6-CHLORO-4-QUINOLINOL;4-Quinolinol, 6-chloro-;6-CHLOROQUINOLIN-4-OL
CAS:23432-43-1
MF:C9H6ClNO
MW:179.6
EINECS:
Product Categories:
Mol File:23432-43-1.mol
6-CHLORO-4-HYDROXYQUINOLINE Structure
6-CHLORO-4-HYDROXYQUINOLINE Chemical Properties
Melting point 269°C(lit.)
Boiling point 348.5±22.0 °C(Predicted)
density 1.412±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
form powder to crystal
pka3.89±0.40(Predicted)
color White to Light gray to Light yellow
InChIKeyXXGUQCVVGPZTPF-UHFFFAOYSA-N
Safety Information
Hazard Codes E,Xn
Risk Statements 22
HS Code 2933499090
MSDS Information
6-CHLORO-4-HYDROXYQUINOLINE Usage And Synthesis
Chemical Propertiesoff White powder
Synthesis
6-Chloro-2,3-Dihydroquinolin-4(1H)-One

21617-20-9

6-CHLORO-4-HYDROXYQUINOLINE

23432-43-1

General procedure for the synthesis of 4-hydroxy-6-chloroquinoline from 6-chloro-4-oxo-2,3-dihydroquinoline: 6-chloro-4-oxo-2,3-dihydroquinoline (0.01 mol) was placed in a 25 mL reaction flask, and 15 mL of acetonitrile and acetic acid (0.01 mol) were added and stirred for 20 min. Subsequently, hydrogen peroxide (0.03 mol) was added slowly and the reaction was stirred at 65 °C. The progress of the reaction was monitored by thin layer chromatography (TLC) and the reaction was terminated after 7 hours. After the reaction solution was cooled to room temperature, it was poured into 50 mL of water, stirred and filtered to obtain the crude product of 4-hydroxy-6-chloroquinoline. The crude product was purified by silica gel column chromatography (silica gel 100-200 mesh, eluent was petroleum ether:ethyl acetate=1:4), and the target component was collected and concentrated to obtain the pure product. The product yield was 88% and purity was 96%.

References[1] Patent: CN108794396, 2018, A. Location in patent: Paragraph 0017
[2] Journal of the American Chemical Society, 1949, vol. 71, p. 1906,1910
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