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ChemicalBook CAS DataBase List 2,6-Dichlorophenol

2,6-Dichlorophenol synthesis

14synthesis methods
2,6-Dichlorophenol has been prepared by the chlorination of phenol with chlorine gas in the presence of nitrobenzene and fuming sulfuric acid, by the decomposition of the diazotate of 2,6-dichloro-4-aminophenol, and by the decarboxylation of 3,5-dichloro-4-hydroxybenzoic acid in quinoline or dimethylaniline.
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Yield:120-83-2 85.43% ,87-65-0 13.31%

Reaction Conditions:

with iron(III) chloride;diphenyl sulfide;boric acid at 40 - 80;

Steps:

3

In a 5,000-liter chlorination kettle with an exhaust gas treatment system, the molar ratio of o-chlorophenol phenol, catalyst diphenyl sulfide, ferric chloride and boric acid (diphenyl sulfide, ferric chloride and boric acid was 1.0 : 1.0: 1.0) Open the water pump, keep the vacuum at -0.005MPa, start to adjust the chlorine speed, the chlorination temperature is maintained at 40 ~ 80 ° C, and start the circulating pump, so that the reaction began to cycle. Until the control analysis found that trichlorophenol ≥ 0.5% can be regarded as the end of dichlorination. And then improve the vacuum to 0.09MPa (away the reaction of the remaining sulfur dioxide and hydrogen chloride), with the pH test paper to detect the tail gas is not significant acid, that is, the end of the catch; and then open the bottom of the discharge valve, the material into the crude phenol in. Gas chromatography analysis revealed 0.54% o-chlorophenol, 0.06% p-chlorophenol, 13.31% 2,6-dichlorophenol, 85.43% 2,4-dichlorophenol and 0.50% of 2,4,6-trichlorophenol.

References:

CN106349025,2017,A Location in patent:Paragraph 0019

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