ChemicalBook > CAS DataBase List > 4-Chloro-2,5-difluoropyridine

4-Chloro-2,5-difluoropyridine

Product Name
4-Chloro-2,5-difluoropyridine
CAS No.
851386-40-8
Chemical Name
4-Chloro-2,5-difluoropyridine
Synonyms
4-Chloro-2,5-difluoropyridine;Pyridine, 4-chloro-2,5-difluoro-
CBNumber
CB01471241
Molecular Formula
C5H2ClF2N
Formula Weight
149.53
MOL File
851386-40-8.mol
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4-Chloro-2,5-difluoropyridine Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Colorless to light yellow Liquid
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Safety

HazardClass 
IRRITANT
HS Code 
2933399090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
C585465
Product name
4-Chloro-2,5-difluoropyridine
Packaging
500mg
Price
$310
Updated
2021/12/16
Matrix Scientific
Product number
054387
Product name
4-Chloro-2,5-difluoropyridine
Purity
88%
Packaging
1g
Price
$345
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0352232
Product name
4-CHLORO-2,5-DIFLUOROPYRIDINE
Purity
95.00%
Packaging
5MG
Price
$502.72
Updated
2021/12/16
AK Scientific
Product number
3167AC
Product name
4-Chloro-2,5-difluoropyridine
Packaging
5g
Price
$986
Updated
2021/12/16
Ambeed
Product number
A257956
Product name
4-Chloro-2,5-difluoropyridine
Purity
95+%
Packaging
100mg
Price
$46
Updated
2021/12/16
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4-Chloro-2,5-difluoropyridine Chemical Properties,Usage,Production

Synthesis

84476-99-3

851386-40-8

General procedure for the synthesis of 4-chloro-2,5-difluoropyridine using 2,5-difluoropyridine as starting material: diisopropylamine (53 g, 0.525 mol) was added to a solvent mixture of tetrahydrofuran (150 ml) and methyl tert-butyl ether (200 ml) under nitrogen protection. The reaction system was cooled to -60 to -40 °C and a hexane solution of n-butyllithium (191 ml, 2.5 M) was slowly added. Subsequently, the reaction temperature was slowly raised to -20°C and stirred at this temperature for 10 minutes. The reaction flask was again cooled to -75 °C and a solution of 2,5-difluoropyridine (50 g, 0.434 mol) was slowly added dropwise for a controlled time of 1 hour. After the dropwise addition was completed, the addition of Freon-113 (89.4 g, 0.478 mol) solution was continued dropwise at -75 °C. After completion of dropwise addition, the reaction system was kept insulated at -75°C for 2 hours. At the end of the reaction, the reaction was quenched with saturated ammonium chloride solution and then the reaction solution was extracted with methyl tert-butyl ether. The organic phase was washed sequentially with 2N aqueous hydrochloric acid solution, water, saturated sodium bicarbonate solution and saturated brine. The organic phase was separated, dried with anhydrous sodium sulfate and filtered. The filtrate was first distilled at 80 °C under atmospheric pressure to remove the low-boiling solvent, then distilled at 120 °C under reduced pressure, and finally distilled at 90 °C under atmospheric pressure to obtain the target product 4-chloro-2,5-difluoropyridine (50 g, 78% yield).

References

[1] Patent: CN106432222, 2017, A. Location in patent: Paragraph 0038; 0039; 0040-0042; 0060-0064; 0079-0083

4-Chloro-2,5-difluoropyridine Preparation Products And Raw materials

Raw materials

Preparation Products

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4-Chloro-2,5-difluoropyridine Suppliers

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