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[ CAS No. 4542-75-0 ] {[proInfo.proName]}

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Chemical Structure| 4542-75-0
Chemical Structure| 4542-75-0
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Product Details of [ 4542-75-0 ]

CAS No. :4542-75-0 MDL No. :MFCD08063928
Formula : C14H12Br2O Boiling Point : -
Linear Structure Formula :- InChI Key :QPSFOUFNVQVKKJ-UHFFFAOYSA-N
M.W : 356.05 Pubchem ID :10269629
Synonyms :

Safety of [ 4542-75-0 ]

Signal Word:Danger Class:8
Precautionary Statements:P260-P264-P270-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P403+P233-P405-P501 UN#:3261
Hazard Statements:H302-H335-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4542-75-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 4542-75-0 ]

[ 4542-75-0 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 100-97-0 ]
  • [ 4542-75-0 ]
  • [ 2215-76-1 ]
  • 2
  • [ 1579-40-4 ]
  • [ 4542-75-0 ]
YieldReaction ConditionsOperation in experiment
93% With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 80 - 90℃; for 6.5h;Inert atmosphere; Prior to use, NBS was recrystallized from water and the carbon tetrachloride was bubbled with nitrogen, stirred for 45 min with sodium sulfate, and checked by 1H-NMR spectroscopy. To a stirred solution of 4,4'-oxybis(methylbenzene) (28) (5.0 g, 25.2 mmol, 1 eq.) and NBS (8.98 g, 50.4 mmol, 2 eq.) in carbon tetrachloride (125 mL) under nitrogen was added a catalytic amount of AIBN. The reaction mixture was heated to 80-90 C (reflux) and stirred for 6.5 h. The solution was then cooled and the succinimide was removed on a sintered glass filter funnel. The solvent was removed in vacuo to yield the desired product 29 as beige crystals (8.3 g, 93%). A portion (1.82 g) was purified by flash chromatography (10:1 hexane:EtOAc) to yield 29 as white crystals: mp 85-86 C (lit.29 mp 93-95 C). 1H NMR (CDCl3): δ 7.38 (d, 4H), 6.98 (d, 4H), 4.52 (s, 4H).
With hydrogen bromide; dihydrogen peroxide; In 1,2-dichloro-ethane; for 12h;Cooling with ice; Irradiation; 82 g (1.2 mol) of 50% hydrogen peroxide was slowly added into a mixture of 109 g (0.55 mol) of 4,4'-oxybis(methylbenzene) and 370 g (2.2 mol) of hydrobromic acid in 1000 g of DCE under ice bath. The resulting mixture was irradiated by a visible light lamp (with a wavelength of about 400 nm) for 12 hours to form a crude product (in an organic layer). 4,4'-oxybis((bromomethyl)benzene) was obtained with a yield of 650% after removing the solvent from the crude product by evaporation.
  • 3
  • [ 4542-75-0 ]
  • [ 194-00-3 ]
  • 2,2'-(oxydibenzyl)bis(2,7-diazapyrenium) dibromide [ No CAS ]
  • 4
  • [ 4542-75-0 ]
  • [ 13925-27-4 ]
  • C46H32N6O3 [ No CAS ]
  • 5
  • [ 4542-75-0 ]
  • [ 2129-89-7 ]
  • bis<4-<2-(diphenylphosphinyl)ethyl>phenyl>ether [ No CAS ]
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