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3,4'-Dichlorodiphenyl ether

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3,4'-Dichlorodiphenyl ether Basic information

Product Name:
3,4'-Dichlorodiphenyl ether
Synonyms:
  • 1-chloro-3-(4-chlorophenoxy)-benzene
  • 2-(2,4-dichlorophenoxy)-N-(1H-1,2,4-triazol-5-yl)acetamide
  • -Dihydroxy-5,6,7-trimethoxyflavylium Chloride
  • 5-Triacetoxy-trans-stilbene &ge
  • -Heptyloxyphenoxymethyl)phenylboronic acid
  • -biphenyl]-2-carboxamide
  • -Hydroxyphenyl)propionic acid-OSu
  • -Dimethyl-4-fluorobiphenyl
CAS:
6842-62-2
MF:
C12H8Cl2O
MW:
239.1
Product Categories:
  • Biphenyl & Diphenyl ether
  • Chlorobenzene Series
Mol File:
6842-62-2.mol
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3,4'-Dichlorodiphenyl ether Chemical Properties

Melting point:
-10 °C
Boiling point:
113°C (0.5 mmHg)
Density 
1.29
refractive index 
1.5950
storage temp. 
Sealed in dry,Room Temperature
InChI
InChI=1S/C12H8Cl2O/c13-9-4-6-11(7-5-9)15-12-3-1-2-10(14)8-12/h1-8H
InChIKey
HPRGYUWRGCTBAV-UHFFFAOYSA-N
SMILES
C1(Cl)=CC=CC(OC2=CC=C(Cl)C=C2)=C1
CAS DataBase Reference
6842-62-2(CAS DataBase Reference)
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3,4'-Dichlorodiphenyl ether Usage And Synthesis

Chemical Properties

Colorless or light yellow oily liquid

Synthesis

106-48-9

541-73-1

6842-62-2

The general steps for synthesizing 3,4'-dichlorodiphenyl ether from p-chlorophenol and 1,3-dichlorobenzene are as follows: first, the organic solvent was prepared by mixing ionic liquid with dipropylene glycol methyl ethyl ether in a mass ratio of 1:20. The specific synthesis method is as follows: (1) A copper salt catalyst is added to the reaction system, while 1,3-dichlorobenzene, p-chlorophenol, a base and the organic solvent prepared above are mixed. Among them, the molar ratio of 1,3-dichlorobenzene, p-chlorophenol, potassium carbonate base and cuprous chloride salt was 6:1:1.2:0.01, and the total dosage of organic solvent was 10% of the total amount of the reactants; (2) under microwave-catalyzed conditions, the reaction mixture was stirred for 2 hours at 500 W power, and the temperature of the reaction was controlled at 60~110°C. The reaction temperature was controlled at 60~110°C. The reaction temperature was set to 0.01 °C for 2 hours. After the reaction was completed, the mixture was left to cool, filtered, and the filtrate was distilled under reduced pressure to collect a colorless and transparent liquid product. The conversion of the method was 99% and the yield was 93%.

References

[1] Patent: CN105198713, 2017, B. Location in patent: Paragraph 0024-0044

3,4'-Dichlorodiphenyl ether Preparation Products And Raw materials

Preparation Products

Raw materials

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