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3,5-Dimethyl-2,6-dibromopyridine

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Products Intro: Product Name:2,6-Dibromo-3,5-dimethylpyridine
CAS:117846-58-9
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Products Intro: Product Name:3,5-dimethyl-2,6-dibromopyridine
CAS:117846-58-9
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Products Intro: Product Name:3,5-Dimethyl-2,6-dibromopyridine
CAS:117846-58-9
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Products Intro: Product Name:2,6-Dibromo-3,5-dimethylpyridine
CAS:117846-58-9
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Products Intro: Product Name:3,5-Dimethyl-2,6-dibromopyridine
CAS:117846-58-9
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3,5-Dimethyl-2,6-dibromopyridine manufacturers

3,5-Dimethyl-2,6-dibromopyridine Basic information
Uses
Product Name:3,5-Dimethyl-2,6-dibromopyridine
Synonyms:3,5-Dimethyl-2,6-dibromopyridine;Pyridine, 2,6-dibromo-3,5-dimethyl-;3,5-Dimethyl-2,6-dibromopyridine ISO 9001:2015 REACH
CAS:117846-58-9
MF:C7H7Br2N
MW:264.95
EINECS:
Product Categories:Heterocycle-Pyridine series
Mol File:117846-58-9.mol
3,5-Dimethyl-2,6-dibromopyridine Structure
3,5-Dimethyl-2,6-dibromopyridine Chemical Properties
Melting point 107-108 °C
Boiling point 303.1±37.0 °C(Predicted)
density 1.795±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-3.07±0.20(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2933399990
MSDS Information
3,5-Dimethyl-2,6-dibromopyridine Usage And Synthesis
Uses3,5-Dimethyl-2,6-dibromopyridine is an important intermediate in organic synthesis, mainly used in pharmaceutical intermediates, organic synthesis, and organic solvents. It can also be used in dye production, pesticide production, and fragrance production.
Synthesis
3,5-Lutidine

591-22-0

3,5-Dimethyl-2,6-dibromopyridine

117846-58-9

The general procedure for the synthesis of 3,5-dimethyl-2,6-dibromopyridine from 3,5-dimethylpyridine was as follows: bromine (Br2, 5.64 mL, 110 mmol) was added dropwise to a fuming sulfuric acid solution (40 mL) of 3,5-dimethylpyridine (5.35 g, 50 mmol) under stirring at 177 K. The reaction was carried out in the following manner. The temperature was maintained and stirring of the reaction mixture was continued for 30 minutes. Subsequently, the reaction system was slowly warmed to 353 K and refluxed at this temperature for 36 hours. Upon completion of the reaction, the solution was cooled to room temperature and slowly poured into water. The reaction mixture was neutralized with aqueous sodium hydroxide (NaOH). The crude product was isolated by filtration. The crude product was purified by column chromatography (eluent: dichloromethane) to yield 3,5-dimethyl-2,6-dibromopyridine (10.71 g, 80% yield) as a white solid with a melting point of 102-103 °C. The product was purified by column chromatography. The structure of the product was confirmed by the following characterization data: 1H NMR (400 MHz, CDCl3): δ 7.35 (s, 1H, pyridinium-H), 2.30 (s, 6H, -CH3); 13C NMR (100 MHz, CDCl3): δ 141.11, 139.51, 134.21, 20.96; IR (KBr, ν, cm- 1): 3132, 1585, 1535, 1386, 1082, 974, 705.

References[1] Tetrahedron Letters, 2013, vol. 54, # 43, p. 5791 - 5794
[2] Tetrahedron Letters, 2013, vol. 54, # 51, p. 7024 - 7028
[3] Journal of the Brazilian Chemical Society, 2016, vol. 27, # 11, p. 1989 - 1997
[4] Acta Crystallographica Section C: Crystal Structure Communications, 2006, vol. 62, # 10, p. o590-o592
3,5-Dimethyl-2,6-dibromopyridine Preparation Products And Raw materials
Raw materials3,5-Lutidine
Tag:3,5-Dimethyl-2,6-dibromopyridine(117846-58-9) Related Product Information
3,5-Lutidine 2,6-Lutidine

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