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32608-29-0

32608-29-0 Structure

32608-29-0 Structure
IdentificationBack Directory
[Name]

2,4-DICHLORO-8-METHOXYQUINOLINE
[CAS]

32608-29-0
[Synonyms]

2,4-DICHLORO-8-METHOXYQUINOLINE
Quinoline, 2,4-dichloro-8-methoxy-
[Molecular Formula]

C10H7Cl2NO
[MDL Number]

MFCD07644554
[MOL File]

32608-29-0.mol
[Molecular Weight]

228.07
Chemical PropertiesBack Directory
[Melting point ]

92 °C
[Boiling point ]

327.9±37.0 °C(Predicted)
[density ]

1.384±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-2.83±0.50(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335-H302
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
Hazard InformationBack Directory
[Synthesis]

Malonic acid

141-82-2

o-Anisidine

90-04-0

2,4-DICHLORO-8-METHOXYQUINOLINE

32608-29-0

The general synthetic route of the compound is schematically described in Scheme 1.The synthesis of 2,4-dichloro-8-methoxyquinoline was carried out with reference to literature reports [27,28] as follows: equimolar o-methoxyaniline and malonic acid were mixed with 30 mL of phosphorochloridic acid and refluxed for 5 h on a heating mantle kept at 80-100°C. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was cooled to room temperature and slowly poured into crushed ice with continuous stirring. The precipitated solid was separated by filtration, dried and washed thoroughly with water. The crude product was purified by column chromatography (eluent ratio 95:5 hexane-ethyl acetate) to afford 2,4-dichloro-8-methoxyquinoline in 78.6% yield.

[References]

[1] Journal of Molecular Structure, 2017, vol. 1131, p. 51 - 72
[2] Research on Chemical Intermediates, 2014, vol. 40, # 5, p. 1851 - 1866
[3] Medicinal Chemistry, 2015, vol. 11, # 8, p. 789 - 797
[4] Organic Process Research and Development, 2016, vol. 20, # 2, p. 215 - 226
[5] Journal of Organic Chemistry, 2013, vol. 78, # 21, p. 10605 - 10616
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