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Chemical Structure| 1094438-61-5 Chemical Structure| 1094438-61-5

Structure of 1094438-61-5

Chemical Structure| 1094438-61-5

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Product Details of [ 1094438-61-5 ]

CAS No. :1094438-61-5
Formula : C9H10Br2O
M.W : 293.98
SMILES Code : CCOC1=CC=C(Br)C=C1CBr
MDL No. :MFCD11180446

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Application In Synthesis of [ 1094438-61-5 ]

* 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 [ 1094438-61-5 ]

[ 1094438-61-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 79636-93-4 ]
  • [ 1094438-61-5 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 3.0h;Reflux; To the previously synthesized ether (4.97 g, 23.1 mmol) in carbon tetrachloride (80 mL) was added N-bromosuccinimide (4.93 g, 27.6 mmol) and benzoyl peroxide (100 mg). The resulting solution was heated to reflux for 3 hrs, allowed to cool, partially evaporated and then filtered. The filtrate was evaporated in vacuo to afford 4-bromo-2-(bromomethyl)-l-ethoxybenzene which could be used without further purification.
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 3.0h;Reflux; Step 2: To a solution of <strong>[79636-93-4]4-bromo-1-ethoxy-2-methylbenzene</strong> (5.0 g, 23.1 mmol) in CCI4 (80 mL) was added N-bromosuccinimide (4.93 g, 27.6 mmol) and benzoyl peroxide (100 mg, cat.). The reaction mixture was then heated to reflux for a period of 3 hrs after which it was allowed to cool, partially evaporated then filtered to remove the succinimide. The filtrate was then evaporated to dryness to afford the benzylbromide which was used without further purification
 

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