FIELD: chemistry.
SUBSTANCE: present invention relates to a method for producing 4-tert-butylpyrocatechin, which is widely used as an inhibitor of polymerization of diene and vinyl aromatic hydrocarbons, as well as a stabilizer of styrene, polymer materials, as antioxidants of oils, waxes and animal fats, in the production of insecticidal compounds. The method consists in the mild oxidation of 4-tert-butylphenol with a solution of a perox compound, as which sodium persulfate is used, in NaOH at a molar ratio of 4-tert-butylphenol: NaOH 1:5 and a molar ratio of 4-tert-butylphenol: sodium persulfate 1:1-1:2. In this case, the oxidation is carried out for 2 hours at a temperature of 20-40°C in the presence of a catalyst, which is used as a catalyst for the interphase transfer of a number of polyethylene glycols from PEG-400 to PEG-2000 in an amount of 5 to 10 wt. % relative to the mass of 4-tert-butylphenol.
EFFECT: simplification of the oxidation process and an increase in the yield of the target product.
1 cl, 1 tbl, 14 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD OF PRODUCING 4-TERT-BUTYL-PYROCATECHOL AND CATALYST FOR ITS PRODUCTION | 2015 |
|
RU2634728C2 |
METHOD OF PREPARING 4-TRETBUTYLPYROCATECHOL | 0 |
|
SU602490A1 |
COMPOSITION INHIBITING POLYMERISATION WHEN PROCESSING LIQUID PYROLYSIS PRODUCTS, METHOD FOR PRODUCTION THEREOF AND METHOD OF INHIBITING POLYMERISATION WHEN PROCESSING LIQUID PYROLYSIS PRODUCTS | 2012 |
|
RU2500660C1 |
METHOD FOR OBTAINING MIXED TRIARYL PHOSPHATES | 2018 |
|
RU2670105C1 |
METHOD OF OBTAINING BENZYLBUTYL ETHER | 2012 |
|
RU2536486C2 |
METHOD FOR PREPARING BETA-(4-HYDROXY-3,5-DI-TERTIARY-BUTYLPHENYL)PROPIONIC ACID METHYL ESTER | 2004 |
|
RU2263104C1 |
METHOD OF PRODUCING 2,6-DI-TERT-BUTYL-P-BENZOQUINONE | 2016 |
|
RU2654477C2 |
METHOD OF PRODUCING SUBSTITUTED PHENOLS, CONTAINING HEM-DICHLOROCYCLOPROPYL SUBSTITUTE | 2010 |
|
RU2430903C1 |
PROCESS FOR PRODUCING PHENOL | 0 |
|
SU1097598A1 |
PROCESS FOR PREPARING 2,4-DI-TERT-BUTYLPHENOL | 0 |
|
SU1035019A1 |
Authors
Dates
2022-08-16—Published
2021-08-02—Filed