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
4-Chloro-2,5-difluoropyridine Property
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- Colorless to light yellow Liquid
Safety
- HazardClass
- IRRITANT
- HS Code
- 2933399090
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.
N-Bromosuccinimide Price
- Product number
- C585465
- Product name
- 4-Chloro-2,5-difluoropyridine
- Packaging
- 500mg
- Price
- $310
- Updated
- 2021/12/16
- Product number
- 054387
- Product name
- 4-Chloro-2,5-difluoropyridine
- Purity
- 88%
- Packaging
- 1g
- Price
- $345
- Updated
- 2021/12/16
- Product number
- HCH0352232
- Product name
- 4-CHLORO-2,5-DIFLUOROPYRIDINE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $502.72
- Updated
- 2021/12/16
- Product number
- 3167AC
- Product name
- 4-Chloro-2,5-difluoropyridine
- Packaging
- 5g
- Price
- $986
- Updated
- 2021/12/16
- Product number
- A257956
- Product name
- 4-Chloro-2,5-difluoropyridine
- Purity
- 95+%
- Packaging
- 5g
- Price
- $630
- Updated
- 2021/12/16
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
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