ChemicalBook--->CAS DataBase List--->40758-65-4

40758-65-4

40758-65-4 Structure

40758-65-4 Structure
IdentificationMore
[Name]

2-ETHOXY-4,6-DICHLOROPYRIMIDINE
[CAS]

40758-65-4
[Synonyms]

2-ETHOXY-4,6-DICHLOROPYRIMIDINE
4,6-DICHLORO-2-ETHOXYPYRIMIDINE
[Molecular Formula]

C6H6Cl2N2O
[MDL Number]

MFCD02262171
[Molecular Weight]

193.03
[MOL File]

40758-65-4.mol
Chemical PropertiesBack Directory
[Boiling point ]

283.5±43.0 °C(Predicted)
[density ]

1.375±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-4.46±0.30(Predicted)
[CAS DataBase Reference]

40758-65-4(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Corrosion (GHS05)
GHS07,GHS05
[Signal word ]

Danger
[Hazard statements ]

H302-H318
[Precautionary statements ]

P280-P305+P351+P338-P310-P264-P270-P301+P312-P330-P501
[REACH Registrations]

Inactive
Questions And AnswerBack Directory
[Application]

2-Ethoxy-4,6-dichloropyrimidine is an important heterocyclic pesticide and pharmaceutical intermediate. It can be used to synthesize highly effective herbicides containing triazole pyrimidine rings, such as dichlorvos and chlorpyrifos; it can also be used to synthesize certain antibiotics. Therefore, 2-ethoxy-4,6-dichloropyrimidine has broad application prospects in organic synthesis, pharmaceuticals, and pesticides.
Hazard InformationBack Directory
[Synthesis]

Sodium ethoxide

141-52-6

4,6-Dichloro-2-(methylsulfonyl)pyrimidine

4489-34-3

2-ETHOXY-4,6-DICHLOROPYRIMIDINE

40758-65-4

To a 500 mL reaction flask equipped with a stirrer and thermometer was added 43.5 g of 2-methylsulfonyl-4,6-dichloropyrimidine (0.19 mol) and 90 g of ethanol and stirred at room temperature. The reaction mixture was then cooled to 0 °C and 130 g of sodium ethanol solution (0.38 mol) at a concentration of 20 wt% was slowly added dropwise. Upon completion of the reaction, the reaction was terminated by sampling and analysis to confirm that the feedstock content was less than 1%. After adjusting the reaction system to neutral pH, a small amount of acetic acid was added and ethanol was recovered under reduced pressure. Subsequently, dichloromethane was added, the solvent was evaporated and water was added to separate the organic layer. The organic layer was washed once with water and the first solvent was recovered. 35.2 g of 2-ethoxy-4,6-dichloropyrimidine was obtained in 95.2% yield and 96.5% purity (HPLC analysis) by distillation under reduced pressure until no liquid was exuded.

[Toxics Screening Level]

The ITSL is being set at the default value of 0.1 μg/m3 with annual averaging.
[References]

[1] Patent: CN106866547, 2017, A. Location in patent: Paragraph 0021; 0022
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