Basic information Safety Supplier Related

2-Bromo-5-formyl-3-methylpyridine

Basic information Safety Supplier Related

2-Bromo-5-formyl-3-methylpyridine Basic information

Product Name:
2-Bromo-5-formyl-3-methylpyridine
Synonyms:
  • 2-Bromo-5-formyl-3-methylpyridine
  • 6-bromo-5-methylnicotinaldehyde
  • 6-BroMo-5-Methyl-pyridine-3-carbaldehyde
  • CML-014
  • 3-Pyridinecarboxaldehyde, 6-bromo-5-methyl-
  • 6-Bromo-5-methyl-3-pyridinecarboxaldehyde
  • KML-12
CAS:
885167-81-7
MF:
C7H6BrNO
MW:
200.03
Product Categories:
  • Boronic Acid
  • Heterocyclic Compounds
Mol File:
885167-81-7.mol
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2-Bromo-5-formyl-3-methylpyridine Chemical Properties

Boiling point:
300.2±42.0 °C(Predicted)
Density 
1.577±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-0.72±0.20(Predicted)
Appearance
Light yellow to yellow Solid
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2-Bromo-5-formyl-3-methylpyridine Usage And Synthesis

Synthesis

4394-85-8

3430-18-0

885167-81-7

The general procedure for the synthesis of 2-bromo-3-methyl-5-formylpyridine from N-formylmorpholine and 2,5-dibromo-3-methylpyridine is as follows: Method 4: Preparation of 6-bromo-5-methylnicotinaldehyde 1. A solution of 2,5-dibromo-3-methylpyridine (5.1 g, 20.30 mmol) in tetrahydrofuran (25 ml) was slowly added dropwise to a solution of 2M isopropylmagnesium chloride (10.7 ml, 21.3 mmol) in tetrahydrofuran which had been pre-cooled to 0 °C at 0 °C. 2. The reaction mixture was stirred at 0°C for 2 hours, followed by continued stirring at room temperature for 1 hour. 3. a solution of tetrahydrofuran (25 ml) of 4-formylmorpholine (2.1 ml, 20.3 mmol) was slowly added dropwise to the reaction mixture, and after completion of the dropwise addition, the reaction mixture was stirred at room temperature for 1 hour. 4. The reaction mixture was poured into water and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure. 5. The residue was purified by fast column chromatography to afford the target product 2-bromo-3-methyl-5-formylpyridine (3.0 g, 74% yield) using isohexane solution of 10% ethyl acetate as eluent. NMR spectrum (DMSO-d6): δ 2.44 (s, 3H), 8.19 (s, 1H), 8.73 (s, 1H), 10.09 (s, 1H).

References

[1] Patent: US2008/119451, 2008, A1. Location in patent: Page/Page column 35
[2] Patent: WO2007/71956, 2007, A1. Location in patent: Page/Page column description
[3] Patent: US2012/184520, 2012, A1. Location in patent: Page/Page column 24

2-Bromo-5-formyl-3-methylpyridineSupplier

Zhuhai Aobokai Biomedical Technology Co., Ltd. Gold
Tel
400-0628126 15697568869;
Email
sales-team@aobchem.com.cn
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Shanghai Ennopharm Co., Ltd.
Tel
+86 (21) 6435-5022
Shanghai Raise Chemical Technology Co.,Ltd
Tel
+86-021-50935922
Anichem Inc.
Tel
0512-69369885
Email
sales@anichem.com.cn
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