Identification | Back Directory | [Name]
3-CHLORO-2-NITROPHENOL | [CAS]
17802-02-7 | [Synonyms]
3-CHLORO-2-NITROPHENOL Phenol, 3-chloro-2-nitro- | [Molecular Formula]
C6H4ClNO3 | [MDL Number]
MFCD08703192 | [MOL File]
17802-02-7.mol | [Molecular Weight]
173.55 |
Chemical Properties | Back Directory | [Melting point ]
37.5 °C | [Boiling point ]
250.8±20.0 °C(Predicted) | [density ]
1.554±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
solid | [pka]
4.45±0.10(Predicted) | [color ]
Yellow-brown |
Hazard Information | Back Directory | [Chemical Properties]
Light yellow crystalline | [Synthesis]
Step i: 2-chloro-6-fluoronitrobenzene (6.62 g, 37.7 mmol) and LiOH-H2O (6.33 g, 151 mmol) were dissolved in a mixed solvent of THF (45 mL) and water (65 mL), followed by the addition of 30% aqueous H2O2 solution (8.60 mL, 80.0 mmol). The resulting turbid solution was sealed and heated to 60°C with vigorous stirring. After 3 days of reaction, the dark orange mixture was cooled and half-saturated aqueous sodium thiosulfate solution (200 mL) was added and vigorously shaken in a split funnel. Subsequently, the mixture was acidified to pH < 3 with 1N HCl, extracted with EtOAc (400 mL + 100 mL) and washed with brine (400 mL). The organic phases were combined, dried with magnesium sulfate, filtered and concentrated to give a dark yellow oil containing a small amount of solid particles (unreacted feedstock) (aminophenol 10b, 6.37 g, 97% yield), which was used directly in the next step of the reaction. | [References]
[1] Patent: WO2009/62285, 2009, A1. Location in patent: Page/Page column 64 [2] Patent: WO2009/62308, 2009, A1. Location in patent: Page/Page column 73-74 [3] Patent: WO2009/62288, 2009, A1. Location in patent: Page/Page column 70-71 [4] Patent: WO2009/62289, 2009, A1. Location in patent: Page/Page column 77-78 [5] Patent: WO2018/37223, 2018, A1. Location in patent: Page/Page column 154 |
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