Identification | Back Directory | [Name]
6-CHLOROQUINOLINE-2-CARBOXYLIC ACID | [CAS]
59394-30-8 | [Synonyms]
AKOS A0602-0951 6-Chloro-2-quinolinecarboxylic acid 6-CHLOROQUINOLINE-2-CARBOXYLIC ACID 2-Quinolinecarboxylic acid, 6-chloro- | [Molecular Formula]
C10H6ClNO2 | [MDL Number]
MFCD09834123 | [MOL File]
59394-30-8.mol | [Molecular Weight]
207.61 |
Chemical Properties | Back Directory | [Melting point ]
228 °C | [Boiling point ]
382.1±27.0 °C(Predicted) | [density ]
1.469±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [pka]
4.45±0.43(Predicted) | [Appearance]
White to yellow Solid |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 6-chloro-2-quinoline carboxylic acid from 6-chloro-2-quinoline carboxaldehyde: A solution of sodium chlorite (2.4 g) and sodium dihydrogen phosphate (2.4 g) in water (24 ml) was added slowly and dropwise over a period of 5 min to a solution of 6-chloroquinoline-2-carboxaldehyde (536 mg; 2.8 mmol) dissolved in a tert-butanol (56 ml) and 2-methyl-2-butene (14 ml) mixed solution. The reaction mixture was stirred at room temperature for 4 hours. After completion of the reaction, the organic solvent was removed by distillation under reduced pressure. Water (30 ml) was added to the residue and a white precipitate was precipitated. The precipitate was collected by filtration, washed with water and dried under vacuum in the presence of phosphorus pentoxide to afford 6-chloroquinoline-2-carboxylic acid in white powder form (505 mg; yield = 87%). Mass spectrometry/liquid chromatography analysis: m/z=208.01 (M+H), retention time=8.55 min (condition 1). NMR hydrogen spectrum (DMSO-d6,400MHz) δ: 8.41-8.39 (m, 1H, aromatic H); 8.20-8.11 (m, 3H, aromatic H); 7.82-7.79 (m, 1H, aromatic H). | [References]
[1] Patent: US2005/154039, 2005, A1. Location in patent: Page/Page column 11 [2] Tetrahedron, 2013, vol. 69, # 38, p. 8209 - 8215 |
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Company Name: |
Cochemical Ltd.
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Tel: |
029-86115547 17791676824 |
Website: |
www.cochemical.com |
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