ChemicalBook--->CAS DataBase List--->101861-61-4

101861-61-4

101861-61-4 Structure

101861-61-4 Structure
IdentificationBack Directory
[Name]

6-CHLORO-3-NITROQUINOLIN-4-OL
[CAS]

101861-61-4
[Synonyms]

6-CHLORO-3-NITROQUINOLIN-4-OL
6-chloro-3-nitro-4-Quinolinol
4-Quinolinol,6-chloro-3-nitro-
6-chloro-3-nitro-1H-quinolin-4-one
[Molecular Formula]

C9H5ClN2O3
[MDL Number]

MFCD09800425
[MOL File]

101861-61-4.mol
[Molecular Weight]

224.6
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

6-CHLORO-3-NITROQUINOLIN-4-OL (101861-61-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzoic acid, 5-chloro-2-[(2-nitroethylidene)amino]-

102014-85-7

6-CHLORO-3-NITROQUINOLIN-4-OL

101861-61-4

Step 2: Synthesis of 6-chloro-3-nitroquinolin-4-ol To a 500 mL round bottom flask was added 5-chloro-2-(2-nitroethylideneamino)benzoic acid (25 g, 0.10 mol), K2CO3 (42.6 g, 0.30 mol) and acetic anhydride (250 mL). The reaction mixture was heated to 90 °C and the reaction was stirred at this temperature for 1 hour. Upon completion of the reaction, the resulting solid product was collected by filtration, washed sufficiently with deionized water to remove residual reactants and salts, and subsequently dried to afford 17.5 g (76% yield) of 6-chloro-3-nitroquinolin-4-ol as a gray solid. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 9.12 (s, 1H), 8.15 (s, 1H), 7.72 (s, 2H). Mass spectral analysis showed m/z: 224 (M+H+).

[References]

[1] Patent: US2010/120741, 2010, A1. Location in patent: Page/Page column 93
[2] Patent: WO2011/112731, 2011, A2. Location in patent: Page/Page column 199-200
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