| Identification | Back Directory | [Name]
4,6-dichloro-2(2H)-Pyridinone | [CAS]
68963-75-7 | [Synonyms]
4,6-dichloropyridin-2-ol 4,6-Dichloropyridin-2(1H)-one 4,6-dichloro-2(2H)-Pyridinone 4,6-DICHLORO-2(1H)-PYRIDINONE 2,4-DICHLORO-6-HYDROXYPYRIDINE 2(1H)-Pyridinone, 4,6-dichloro- 4,6-dichloro-1,2-dihydropyridin-2-one | [Molecular Formula]
C5H3Cl2NO | [MDL Number]
MFCD18803554 | [MOL File]
68963-75-7.mol | [Molecular Weight]
163.99 |
| Chemical Properties | Back Directory | [Melting point ]
151℃ | [Boiling point ]
275.9±40.0 °C(Predicted) | [density ]
1.52±0.1 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
5.85±0.10(Predicted) | [Appearance]
Off-white to light yellow Solid |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 4,6-dichloro-2-hydroxypyridine from 2-amino-4,6-dichloropyridine: A solution of sodium nitrite (64 mg, 0.93 mmol) dissolved in water (0.6 mL) was added dropwise to a stirred solution of 2-amino-4,6-dichloropyridine (126 mg, 0.77 mmol) in a 5% aqueous sulfuric acid solution (5 mL) at 0 °C. in aqueous 5% sulfuric acid (5 mL), and the time of dropwise addition was controlled within 5 min. The reaction mixture was continued to be stirred at 0 °C for 1 hour. Subsequently, the reaction solution was diluted with deionized water (20 mL) and extracted with dichloromethane (3 x 20 mL). The organic phases were combined, washed with saturated saline (20 mL), dried over anhydrous magnesium sulfate and concentrated under reduced pressure to afford the target product 2,4-dichloro-6-hydroxypyridine (116 mg, 0.71 mmol, 92% yield). Mass spectrum (ESI) m/z: 164,166 [M+H]+. | [References]
[1] Patent: US2007/185156, 2007, A1. Location in patent: Page/Page column 11 [2] Patent: WO2007/39563, 2007, A1. Location in patent: Page/Page column 27 [3] Patent: US2007/112019, 2007, A1. Location in patent: Page/Page column 14/1 [4] Patent: WO2007/63071, 2007, A1. Location in patent: Page/Page column 24 [5] Journal fuer Praktische Chemie (Leipzig), 1932, vol. 133, p. 36,43 |
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