Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Methylpyridine >  3,5-Dichloro-4-Picoline

3,5-Dichloro-4-Picoline

Basic information Safety Supplier Related

3,5-Dichloro-4-Picoline Basic information

Product Name:
3,5-Dichloro-4-Picoline
Synonyms:
  • 3,5-Dichloro-4-methylpyridine 97%
  • Pyridine,3,5-dichloro-4-Methyl-
  • 3,5-Dichloro-4-Picoline
  • 3,5-Dichloro-4-methylpyridine
  • 3,5-Dichloro-4-Picoline ISO 9001:2015 REACH
CAS:
100868-46-0
MF:
C6H5Cl2N
MW:
162.02
EINECS:
688-519-4
Product Categories:
  • pharmacetical
  • Pyridine
Mol File:
100868-46-0.mol
More
Less

3,5-Dichloro-4-Picoline Chemical Properties

Melting point:
49 °C
Boiling point:
125-127 °C(Press: 74 Torr)
Density 
1.319±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
0.62±0.10(Predicted)
Appearance
Off-white to light brown Solid
InChI
InChI=1S/C6H5Cl2N/c1-4-5(7)2-9-3-6(4)8/h2-3H,1H3
InChIKey
YBHYECGRNFZJPC-UHFFFAOYSA-N
SMILES
C1=NC=C(Cl)C(C)=C1Cl
More
Less

Safety Information

HS Code 
2933399990
More
Less

3,5-Dichloro-4-Picoline Usage And Synthesis

Synthesis

2457-47-8

74-88-4

100868-46-0

Example 6 (Scheme 1) Preparation of 3,5-dichloro-4-methylpyridine (4): diisopropylamine (70 mL, 500 mmol) was dissolved in anhydrous tetrahydrofuran (500 mL) under nitrogen protection, and the resultant solution was cooled to -10 °C and n-butyllithium (2.5 M hexane solution, 210 mL, 525 mmol) was added slowly dropwise under stirring. After the dropwise addition, stirring was continued for 30 min at -10 °C. Subsequently, the reaction system was further cooled to -20 °C and a tetrahydrofuran (200 mL) solution of 3,5-dichloropyridine (66.6 g, 450 mmol) was slowly added dropwise. After the dropwise addition was completed, the reaction mixture was stirred at -10 °C for 30 min. Next, the reaction system was cooled to -70 °C and a tetrahydrofuran (100 mL) solution of iodomethane (50 mL, 1.6 mol) was added dropwise. After the dropwise addition, the reaction mixture was slowly warmed up to room temperature. Upon completion of the reaction, the reaction was quenched with deionized water (100 mL) and extracted with ether (3 x 100 mL). The organic layers were combined, dried over anhydrous sodium sulfate (5 g), filtered and concentrated to dryness under reduced pressure. The crude product was recrystallized by two recrystallizations from aqueous ethanol followed by hexane to give 3,5-dichloro-4-methylpyridine (49.9 g, 306 mmol, 68% yield) as a white solid.

References

[1] Patent: EP2070913, 2009, A1. Location in patent: Page/Page column 18
[2] Patent: EP2022783, 2009, A1. Location in patent: Page/Page column 12
[3] Journal of Medicinal Chemistry, 2014, vol. 57, # 3, p. 793 - 816

3,5-Dichloro-4-PicolineSupplier

Shanghai Hekang Biotechnology Co., Ltd. Gold
Tel
18939837085
Email
youchemicals@gmail.com
PharmaBlock Sciences (Nanjing),Inc.
Tel
025-86918202 4000255188
Email
sales@pharmablock.com
ShangHai DEMO Chemical Co.,Ltd
Tel
400-021-7337 2355568890
Email
sales@demochem.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com