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3,5-Dichloro-2,4,6-trifluoropyridine

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3,5-Dichloro-2,4,6-trifluoropyridine Basic information

Product Name:
3,5-Dichloro-2,4,6-trifluoropyridine
Synonyms:
  • LABOTEST-BB LT00848192
  • 3,5-DICHLOROTRIFLUOROPYRIDINE
  • 3,5-DICHLORO-2,4,6-TRIFLUOROPYRIDINE
  • 2,4,6-TRIFLUORO-3,5-DICHLOROPYRIDINE
  • 2,6-DICHLORO-1,3,5-TRIFLUOROBENZENE
  • 3,5-DICHLORO-2,4,6-TRIFLUOROPYRIDINE, 98 %
  • 3,5-DICHLORO-2,4,6-TRIFLUOROPYRIDINE, 97+%
  • 3,5-Dichloro-2,4,6-trifluoropyridine 98%
CAS:
1737-93-5
MF:
C5Cl2F3N
MW:
201.96
EINECS:
217-088-3
Product Categories:
  • Building Blocks
  • C5
  • C5 to C6
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Heterocyclic Fluorinated Building Blocks
  • Other Fluorinated Heterocycles
  • C5Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyridines
  • Pyridines, Pyrimidines, Purines and Pteredines
  • Fluorin-contained pyridine series
  • Pyridine
Mol File:
1737-93-5.mol
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3,5-Dichloro-2,4,6-trifluoropyridine Chemical Properties

Melting point:
23-24 °C
Boiling point:
159-160 °C(lit.)
Density 
1.622 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.478(lit.)
Flash point:
>230 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-4.30±0.10(Predicted)
Specific Gravity
1.622
BRN 
475874
InChI
InChI=1S/C5Cl2F3N/c6-1-3(8)2(7)5(10)11-4(1)9
InChIKey
PKSORSNCSXBXOT-UHFFFAOYSA-N
SMILES
C1(F)=NC(F)=C(Cl)C(F)=C1Cl
CAS DataBase Reference
1737-93-5(CAS DataBase Reference)
NIST Chemistry Reference
Pyridine, 3,5-dichloro-2,4,6-trifluoro-(1737-93-5)
EPA Substance Registry System
Pyridine, 3,5-dichloro-2,4,6-trifluoro- (1737-93-5)
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Safety Information

Hazard Codes 
Xi,T,T+
Risk Statements 
36/37/38-26
Safety Statements 
26-37/39-36-45-36/37-28
RIDADR 
UN 3382 6.1/PG 1
WGK Germany 
3
Hazard Note 
Toxic
TSCA 
TSCA listed
HazardClass 
6.1
PackingGroup 
II

MSDS

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3,5-Dichloro-2,4,6-trifluoropyridine Usage And Synthesis

Chemical Properties

Clear colorless to pale yellow liquid

General Description

A colorless liquid. Insoluble in water and denser than water. Hence sinks in water. Contact may irritate skin, eyes, and mucous membranes. Very toxic by ingestion, inhalation and skin absorption. Used to make other chemicals.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

3,5-DICHLORO-2,4,6-TRI-FLUOROPYRIDINE is a halogenated amine. Behaves as a weak chemical base, neutralizing acids in exothermic reactions. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

Health Hazard

Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Containers may explode when heated. Runoff may pollute waterways.

Synthesis

2176-62-7

1737-93-5

The general procedure for the synthesis of 3,5-dichloro-2,4,6-trifluoropyridine from pentachloropyridine (2,3,4,5,6-pentachloropyridine) was as follows: in a 1000mL three-necked flask, 600mL of DMI (1,3-dimethyl-2-imidazolidinone) and 146.72g of anhydrous KF (potassium fluoride) (purity of 99%, particle size of 20-50 μm) were added. 60 g of solvent was removed by stirring distillation under reduced pressure (130-135 °C/60 mmHg), and the system was heated to 90 °C after the moisture content was determined to be less than 1000 ppm by water evaporation. Subsequently, 129.40 g of pentachloropyridine of 97% purity was added, the reaction temperature was maintained at 90 °C and stirred for 1.5 hours. Upon completion of the reaction, the heating was stopped and the reaction mixture was cooled to room temperature. The reaction mixture was filtered and the filtrate and solid residue were obtained by separation. The solid residue was washed with 100 mL of DMI and diafiltrated to obtain the wash solution. The wash solution and initial filtrate were combined and a distillation operation was carried out to collect the fractions at a pressure of 65-70.5 KPa to obtain the target product 3,5-dichloro-2,4,6-trifluoropyridine.

References

[1] Patent: CN106008331, 2016, A. Location in patent: Paragraph 0059; 0063
[2] Patent: CN108017574, 2018, A. Location in patent: Paragraph 0040-0043; 0052
[3] Journal of the Chemical Society - Perkin Transactions 1, 1997, # 24, p. 3623 - 3627
[4] Russian Chemical Bulletin, 2007, vol. 56, # 11, p. 2239 - 2246
[5] Patent: CN106187872, 2016, A. Location in patent: Paragraph 0027; 0028; 0029

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