3,4'-Dichlorodiphenyl ether
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
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)
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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3,4'-Dichlorodiphenyl ether(6842-62-2)Related Product Information
- 1,2-Dichloro-4-(chloromethyl)benzene
- Diphenyl ether
- Ethylbenzene
- Triclosan
- 4,4'-Oxybisbenzoic acid
- C8E3
- 2-Chlorodiphenyl ether
- 2,4-Dichlorophenol
- Allylbenzene
- 2',4'-Dichloroacetophenone
- 4,4'-Dichlorodiphenyl sulfone
- 2-Hydroxy-4,4'-dichlorodiphenyl ether
- Benzene
- Difluorochloromethane
- 4-ACETYL-3,4'-DICHLORODIPHENYL ETHER
- Sodium 2-amino-4,4'-dichlorodiphenylether-2'-sulfonate
- Diethyl ether
- 4-ACETYL-2'',4''-DICHLORODIPHENYL ETHER