97416-84-7Relevant articles and documents
Preparation method of methyl octabromoether
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Paragraph 0017; 0021-0030, (2021/10/27)
The invention belongs to the technical field of organic synthesis, and particularly relates to a preparation method of methyl octabromoether. Tetrabromobisphenol A-bis (2-methyl)allyl ether is used as a raw material, the methyl octabromoether is prepared under a catalytic system of N-bromosuccinimide (NBS), an auxiliary agent and a catalyst, the yield is greater than or equal to 98.6%, and the purity is greater than or equal to 99.0%. The preparation method is a method for synthesizing the methyl octabromoether, wherein the method is simple and convenient to operate and high in selectivity, bromine does not need to be used as an initial raw material, and the process safety is better; and the product yield is high, and the product quality is good.
Preparation method of high-purity methyl octabromoether
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Paragraph 0023-0040, (2021/05/26)
The invention provides a preparation method of high-purity methyl octabromoether, which comprises the following steps of: (1) adding tetrabromobisphenol A and caustic soda flakes into a solvent A, stirring until the tetrabromobisphenol A and the caustic soda flakes are completely dissolved, adding a high-efficiency catalyst A, dropwise adding methyl chloropropene for reaction, and filtering after the reaction is completed to obtain an intermediate product methyl tetrabromoether; (2) adding the methyl tetrabromoether prepared in the step (1) into a solvent B, stirring for dissolving, washing and separating water after the materials are completely dissolved, adding a high-efficiency catalyst B, and dropwise adding liquid bromine to obtain a solution containing methyl octabromoether; and (3) neutralizing the solution containing methyl octabromoether with a sodium sulfite solution, washing with water, separating water, distilling, crystallizing, filtering and drying to obtain the methyl octabromoether. The purity of the prepared methyl octabromoether is improved to 98% or above, and the methyl octabromoether can be added to prepare XPS flame-retardant master batch with a high flame-retardant effect and has a better application prospect.
Synthesis method of 2,2-bis[3,5-dibromo-4-(2,3-dibromo-2-methylpropoxy)phenyl]propane
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Paragraph 0043-0053, (2019/12/02)
The invention relates to the technical field of flame retardants, and provides a synthesis method of 2,2-bi[3,5-dibromo-4-(2,3-dibromo-2-methylpropoxy)phenyl]propane, which comprises the following steps: mixing 2,2-bis[4-(2-methylallyloxy)phenyl]propane,
Preparation method for flame retardant of 2,2-bis [3,5-dibromo-4-(2,3-dibromo-2-methyl propoxy) phenyl] propane
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Paragraph 0021, (2016/11/28)
The invention relates to a synthetic preparation method for a brominated flame retardant, namely, 2,2-bis [3,5-dibromo-4-(2,3-dibromo-2-methyl propoxy) phenyl] propane. According to the preparation method, bisphenol A, 3-halogenated methyl propylene and a
Method for preparing methyl octabromo-ether flame retardant
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Paragraph 0036; 0037, (2016/11/17)
The invention discloses a method for preparing a methyl octabromo-ether flame retardant. The method comprises the following steps: enabling bisphenol A and an etherifying agent to have etherification reaction so as to generate a bisphenol A diallyl ether
Bromine-containing organic compounds, bromine-containing organic compound-containing composition and method of manufacturing the same
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Paragraph 0042-0056, (2020/11/05)
PROBLEM TO BE SOLVED: To provide a bromine-containing organic compound which imparts high flame retardancy and thermal stability to a resin when it is compounded with the resin. SOLUTION: The bromine-containing organic compound is represented by formula (1), a flame retardant contains the bromine-containing organic compound, and a flame retardant resin composition contains the flame retardant and a resin. In formula, A represents one of -CH2-, -C(CH3)2-, and -S-, each of R1and R2represents a hydrogen atom or a 1-6C saturated hydrocarbon group, R3represents a 1-6C saturated hydrocarbon group, Y represents a halogen atom, and each of m and n represents an integer of 1-4. COPYRIGHT: (C)2013,JPOandINPIT
Bromine compound production method
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, (2008/06/13)
Method of producing a bromine compound having an aliphatic unsaturated bond which includes reacting a compound having an aliphatic unsaturated bond represented by the following general formula (1) with bromine: to produce a bromine compound represented by the following formula (2): wherein Ar1, Ar2 and Y are the same as defined in the above general formula (1) , and R3 and R4 are groups obtained by saturating the unsaturated groups of R1 and R2 in the above general formula (1) with bromine, respectively. The reaction is carried out in the presence of a solvent which is inactive in the reaction, and a substantial amount of the heat of reaction is removed from a reaction system by the vaporization of the solvent or bromine. A high-purity bromine compound in high yield which is useful as flame retardant, can be obtained.
Bromine compound production method
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, (2008/06/13)
A high-purity bromine compound which is useful as flame retardant, can be obtained industrially advantageously by a process comprising reacting bromine with an aliphatically unsaturated compound of formula (1) : R1-O-Ar1-Y-Ar2-O-R2to produce a bromine compound of formula (2): R3-O-Ar1-Y-Ar2-O-R4wherein in each formula Ar1and Ar2are independently a C5-16aromatic hydrocarbon or a C5-12saturated alicyclic hydrocarbon, and Y is a C1-6saturated hydrocarbon, a sulfone, sulfide, ketone or C2-6alkylene oxide or is a single bond; R1and R2are each independently a C2-11hydrocarbon group which is at least partially unsaturated; and R3and R4are groups obtained by saturating with a bromine atom the unsaturated groups of R1and R2respectively, wherein the reaction is carried out in the presence of a solvent which is inactive in the reaction, and a substantial amount (e.g. 80% or more) of reaction heat is removed from the reaction system by the vaporization heat of the solvent or bromine.
