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Chemical Structure| 18087-51-9 Chemical Structure| 18087-51-9

Structure of 18087-51-9

Chemical Structure| 18087-51-9

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Product Details of [ 18087-51-9 ]

CAS No. :18087-51-9
Formula : C9H10BrNO2
M.W : 244.09
SMILES Code : O=[N+](C1=C(C)C(Br)=C(C)C(C)=C1)[O-]

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Application In Synthesis of [ 18087-51-9 ]

* 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 [ 18087-51-9 ]

[ 18087-51-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 610-91-3 ]
  • [ 18087-51-9 ]
YieldReaction ConditionsOperation in experiment
83% With N-Bromosuccinimide; iron; trifluoroacetic acid; at 75℃; for 72.0h; To a solution of <strong>[610-91-3]1,2,4-trimethyl-5-nitrobenzene</strong> (62) (2.0 g, 12.1 mmol) in trifluoroacetic acid (24 mL) was added NBS (1.2 g, 6.7 mmol) and iron (20 mg, 0.4 mmol). The reaction mixture was heated at 75 C. for 3 days, allowed to cool to room temperature and then the solvent was removed under reduced pressure. The resultant residue was dissolved in EtOAc and washed with aqueous saturated sodium bicarbonate, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified over silica gel and eluted with 0-5% EtOAc/heptane and gave 3-bromo-<strong>[610-91-3]1,2,4-trimethyl-5-nitrobenzene</strong> (63) as a white solid (1.4 g, 83% yield). 1H NMR (400 MHz, CDCl3) δ 7.55 (s, 1H), 2.57 (s, 3H), 2.47 (s, 3H), 2.39 (s, 3H).
With ferric(III) bromide; bromine; iron; In 1,2-dichloro-ethane; at 40℃; for 12.0h; To a mixture of l,2,4-trimethyl-5- nitrobenzene (10 g, 60.5 mmol, 1 eq ) and DCE (200 mL) were added FeBr3 (358 mg, 1.21 mmol, 0.02 eq ), Fe (879 mg, 15.7 mmol, 0.26 eq) and Bn (24.2 g, 151 mmol, 7.80 mL, 2.5 eq) in one portion at 25 C. The mixture was heated to 40 C and stirred for 12 hours. The mixture was cooled to 25C and added saturated Na2SC>3 (200 mL). The mixture was separated, and the aqueous phase was extracted with ethyl acetate (3 c 200 mL). The combined organic layers were washed with brine (200 mL). The combined organic layers were dried over anhydrous Na2SC>4, filtered and concentrated under vacuum to give the title compound (17 g, crude). Yellow solid.
 

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