Identification | Back Directory | [Name]
3-Bromo-5-ethoxypyridine | [CAS]
17117-17-8 | [Synonyms]
5-bromo-3-ethoxypyridine Pyridine, 3-broMo-5-ethoxy- | [Molecular Formula]
C7H8BrNO | [MDL Number]
MFCD00234116 | [MOL File]
17117-17-8.mol | [Molecular Weight]
202.06 |
Chemical Properties | Back Directory | [Melting point ]
9°C(lit.) | [Boiling point ]
240°C(lit.) | [refractive index ]
1.5540 to 1.5580 | [storage temp. ]
Room temperature. | [form ]
clear liquid | [color ]
Colorless to Light orange to Yellow |
Hazard Information | Back Directory | [Synthesis]
Sodium metal (4.60 g, 200 mmol) was added in batches to anhydrous ethanol (100 mL) under nitrogen protection, keeping the reaction temperature at 0-5 °C. The mixture was stirred to slowly warm up to room temperature over 18 hours. Subsequently, 3,5-dibromopyridine (31.5 g, 133 mmol) and N,N-dimethylformamide (DMF, 100 mL) were added to the reaction system. The reaction mixture was heated to 70 °C with continuous stirring for 48 hours. After completion of the reaction, the brown mixture was cooled to room temperature, slowly poured into water (600 mL) and extracted with ether (3 x 500 mL). The ether extracts were combined, dried with anhydrous sodium sulfate, filtered and concentrated by rotary evaporator. The final product was purified by vacuum distillation to give 22.85 g (85.0% yield) of 5-bromo-3-ethoxypyridine as an oil with a boiling point of 89-90 °C (2.8 mmHg). A boiling point of 111 °C (5 mmHg) has been reported in the literature (see K. Clarke et al., J. Chem. Soc. 1885 (1960)). | [References]
[1] Patent: WO2006/23630, 2006, A2. Location in patent: Page/Page column 60 [2] Journal of Medicinal Chemistry, 2009, vol. 52, # 14, p. 4126 - 4141 [3] Patent: WO2010/96389, 2010, A1. Location in patent: Page/Page column 37; 39 [4] Patent: WO2010/135014, 2010, A1. Location in patent: Page/Page column 45-47 [5] Patent: WO2011/87776, 2011, A1. Location in patent: Page/Page column 48; 51 |
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Heterochem
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www.hetero-chem.com |
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