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Chemical Structure| 880348-24-3 Chemical Structure| 880348-24-3

Structure of 880348-24-3

Chemical Structure| 880348-24-3

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Product Details of [ 880348-24-3 ]

CAS No. :880348-24-3
Formula : C7H5Br2Cl
M.W : 284.38
SMILES Code : ClC1=C(Br)C=C(CBr)C=C1
MDL No. :MFCD08059086

Safety of [ 880348-24-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:8
UN#:1759
Packing Group:

Application In Synthesis of [ 880348-24-3 ]

* 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 [ 880348-24-3 ]

[ 880348-24-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 57310-39-1 ]
  • [ 880348-24-3 ]
YieldReaction ConditionsOperation in experiment
47% With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 4h;Reflux; Step 1: <strong>[57310-39-1]3-Bromo-4-chlorotoluene</strong> (1.0 equiv, 3.0 g, 14.6 mmol) and N-bromosuccinimide (1.2 equiv., 3.1 g, 17.5 mmol) were dissolved in CCl4, AIBN (0.01 equiv., 23.9 mg, 0.15 mmol) was added and the mixture was stirred under reflux for 4 h. After cooling to room temperature, the mixture was washed with sat. NaHCO3 solution and with water, the organic phase was concenrtated and the residue was purified by column chromatography (EtOAc/heptane gradient). This gave 2.0 g (47% of theory) of 2-bromo-4-bromomethyl-1-chlorobenzene.
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 16h;Reflux; General procedure: A mixture of bromotoluene intermediate 7-14 or 16 (10 mmol), N-bromosuccinimide (15 mmol, 2.67 g) and azobisisobutyronitrile (5 mmol, 82 mg) in tetrachloromethane (20 mL) was refluxed for 16 h. After cooling the mixture was filtered, the filtrate was diluted with dichloromethane (30 mL), washed with water (50 mL) and brine (50 mL), dried over anhydrous Na2SO4 and evaporated. The residue containing the adequate benzyl bromide derivative without further purification was used to the next step.
 

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