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Chemical Structure| 856935-35-8 Chemical Structure| 856935-35-8

Structure of 856935-35-8

Chemical Structure| 856935-35-8

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Product Details of [ 856935-35-8 ]

CAS No. :856935-35-8
Formula : C8H5BrFN
M.W : 214.03
SMILES Code : FC1=C(CBr)C=C(C=C1)C#N
MDL No. :MFCD08275458

Safety of [ 856935-35-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 856935-35-8 ]

* 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 [ 856935-35-8 ]

[ 856935-35-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 185147-08-4 ]
  • [ 856935-35-8 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 0.5h;Heating / reflux; Irradiation; 3-(bromomethyl)-4-fluorobenzonitrileTo a solution of <strong>[185147-08-4]4-fluoro-3-methylbenzonitrile</strong> (15.0 g, 111 mmol), in CCl4 (600 mL) was added N-bromosuccinimide (23.7 g, 133 mmol), and benzoyl perioxide (5.38 g, 22.2 mol). The mixture was irradiated with a sunlamp (250 W) to create a gentle reflux. After 0.5 hours of exposure the reaction was complete by TLC. The reaction mixture was cooled and filtered through celite. The filtrate was condensed in vacou to yield brown oil. The crude residue was purified via silica gel column chromatography (hexanes/ethyl acetate) to yield 17.7 g of the desired product. 1HNMR(CDCl3) delta : 7.78 (d, IH), 7.65 (m, IH), 7.20 (t, IH), 4.48 (s, 2H).
 

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