| Identification | Back Directory | [Name]
5-BROMO-2-METHOXY-3-METHYLPYRIDINE | [CAS]
760207-87-2 | [Synonyms]
5-Bromo-3-methyl-2-methoxypyridine
Pyridine, 5-broMo-2-Methoxy-3-Methyl-
5-Bromo-2-methoxy-3-methylpyridine 97%
5-BROMO-2-METHOXY-3-METHYLPYRIDINE ISO 9001：2015 REACH | [Molecular Formula]
C7H8BrNO | [MDL Number]
MFCD07375124 | [MOL File]
760207-87-2.mol | [Molecular Weight]
202.05 |
| Chemical Properties | Back Directory | [Boiling point ]
217.8±35.0 °C(Predicted) | [density ]
1.452g/ml | [refractive index ]
1.5540 | [storage temp. ]
Room temperature. | [pka]
1.33±0.20(Predicted) | [Appearance]
Colorless to light yellow Liquid |
| Hazard Information | Back Directory | [Synthesis]
A) Synthesis of 5-bromo-2-methoxy-3-methylpyridine. 2,5-Dibromo-3-methylpyridine (2.08 g, 8.3 mmol) was suspended in a methanolic solution (17 mL) of 2 M sodium methanol and heated by single mode microwave radiation at 120 °C for 40 min. After completion of the reaction, the reaction mixture was slowly poured into a mixture of ice and 1 M aqueous hydrochloric acid solution and extracted twice with dichloromethane. The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the crude product 5-bromo-2-methoxy-3-methylpyridine 1.57 g (89% yield), which could be used in the subsequent reaction without further purification. The product was characterized by 1H NMR (400 MHz, with chloroform-d as solvent and internal standard): δ 8.02 (d, 1H, J = 2.3 Hz), 7.45-7.47 (m, 1H), 3.92 (s, 3H), 2.16 (broad single peak, 3H). | [References]
[1] Patent: WO2007/8143, 2007, A1. Location in patent: Page/Page column 48
[2] Patent: WO2007/8146, 2007, A1. Location in patent: Page/Page column 42-43
[3] Patent: US2015/25087, 2015, A1. Location in patent: Paragraph 0168; 0230; 0231 |
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