ChemicalBook CAS DataBase List 2-BROMODIBENZOTHIOPHENE

2-BROMODIBENZOTHIOPHENE synthesis

4synthesis methods

Product Name:2-BROMODIBENZOTHIOPHENE
CAS Number:22439-61-8
Molecular formula:C12H7BrS
Molecular Weight:263.15

132-65-0 Synthesis

132-65-0
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$6.00/5g

22439-61-8
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$6.00/1g

Yield:22439-61-8 93.18%

Reaction Conditions:

with N-Bromosuccinimide in water;1,2-dichloro-ethane at 10; pH=3; for 12 h;pH-value;Reagent/catalyst;Temperature;Solvent;

Steps:

1-3; 1-2

9.2 g of dibenzothiophene was placed in a 500-ml three-necked round flask, and 150 ml of ethylene chloride was added. The dibenzothiophene was dissolved in a magnetic stirrer and the internal temperature of the reaction solution was adjusted to 10 ° C. 10.7 g of N-bromosuccinimide and 3 g of acid clay were added to the reaction solution and the reaction was started for 6 hours. At this time, the acid clay corresponds to about 32.6 wt% of dibenzothiophene. The acid clay was pH 3 (pH in 10% aqueous solution). After 6 hours of reaction, To the solution containing the reaction solution, N-bromosuccinimide and acid clay, 150 ml of a 5% aqueous sodium hydrogencarbonate solution was added and stirred for 1 hour to separate layers. Thereafter, the organic layer is washed twice with water, and then all of the solvent is distilled off to produce a solid. FIG. 3 is a graph showing the result of a solid produced by the above production method at a wavelength of 254 nm using HPLC. As shown in FIG. 3, The solid component was 96.71% by weight of the product, 2-bromodibenzothiophene, It can be confirmed that the by-product is composed of 2.21% by weight, the starting material is dibenzothiophene is 0.01% by weight and other substances. 300 m? of acetonitrile was added to the solid, and the dissolution temperature was raised to 82 ° C to dissolve the solution. The solution was cooled down to 30 ° C and cooled to remove the precipitated solid. The precipitated solid is a by-product 2,7-dibromodibenzothiophene.310 ml of acetonitrile in the filtrate was distilled off and then cooled to room temperature. The resulting solid was filtered to obtain 12.3 g (yield: 93.18%) of 2-bromodibenzothiophene having a purity of 99% or more.

References:

KR101906794,2018,B1 Location in patent:Paragraph 0045; 0065; 0090-0144

132-65-0 Synthesis

132-65-0
377 suppliers
$6.00/5g

22439-61-8
248 suppliers
$6.00/1g

31574-87-5 Synthesis