Identification | Back Directory | [Name]
4,4'-DIBROMO DIPHENYL SULFONE | [CAS]
2050-48-8 | [Synonyms]
4,4'-Dibromo dipheny 4-bromophenyl sulfone BIS(4-BROMOPHENYL)SULFONE BIS(4-BROMOPHENYL)SULPHONE Bis(p-bromophenyl) sulfone Sulfone, bis(p-bromophenyl) BIS(4-BROMOPHENYL)SULFPHONE 4,4`-Dibromodiphenylsulphone 4,4'-DIBROMO DIPHENYL SULFONE 4,4'-sulfonylbis(broMobenzene) Benzene, 1,1'-sulfonylbis(4-bromo- Sulfonylbis(1,4-phenylene) dibromide 1-Bromo-4-[(4-bromophenyl)sulfonyl]benzene TIANFUCHEM--2050-48-8--4,4'-DIBROMO DIPHENYL SULFONE in stock | [Molecular Formula]
C12H8Br2O2S | [MDL Number]
MFCD00017836 | [MOL File]
2050-48-8.mol | [Molecular Weight]
376.06 |
Chemical Properties | Back Directory | [Melting point ]
172°C | [Boiling point ]
455.7±30.0 °C(Predicted) | [density ]
1.8800 | [storage temp. ]
2-8°C | [Appearance]
Off-white to light brown Solid |
Safety Data | Back Directory | [Symbol(GHS) ]
 GHS07 | [Signal word ]
Warning | [Hazard statements ]
H319 | [Precautionary statements ]
P305+P351+P338 | [Toxicity]
mouse,LD50,intravenous,320mg/kg (320mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#01239, |
Hazard Information | Back Directory | [Synthesis]
4-Bromobenzenesulfonyl chloride (5.00 g, 19.69 mmol) and bromobenzene (4.61 g, 29.54 mmol) were added to a 250 mL three-necked flask and dissolved in 40 mL of dichloromethane. Ferric chloride (6.34 g, 39.39 mmol) was then added and the reaction mixture was heated to 40 °C and stirred for 6 hours. Upon completion of the reaction, the reaction solution was cooled to room temperature and 30 mL of dichloromethane and 50 mL of 1 M hydrochloric acid solution were slowly added and stirring was continued for 10 minutes. The mixture was transferred to a partition funnel and the organic layer was separated. The aqueous layer was extracted three times with dichloromethane and the organic layers were combined. The organic layer was dried with anhydrous sodium sulfate and filtered. The filtrate was concentrated by rotary evaporation to obtain the crude product. The crude product was purified by silica gel column chromatography, and the eluent was a solvent mixture of hexane and dichloromethane (4:5, v/v). The final product was dried under vacuum to give 4,4'-dibromodiphenyl sulfone (6.48 g, 88% yield) in white powder form. | [References]
[1] Patent: CN108084150, 2018, A. Location in patent: Paragraph 0086; 0087; 0088; 0089 [2] Recueil des Travaux Chimiques des Pays-Bas, 1910, vol. 29, p. 324 [3] Recueil des Travaux Chimiques des Pays-Bas, 1911, vol. 30, p. 139 [4] Recueil des Travaux Chimiques des Pays-Bas, 1914, vol. 33, p. 130,152 [5] Chem. Zentralbl., 1914, vol. 85, # I, p. 2166 |
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