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[ CAS No. 162100-99-4 ] {[proInfo.proName]}

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Chemical Structure| 162100-99-4
Chemical Structure| 162100-99-4
Structure of 162100-99-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 162100-99-4 ]

CAS No. :162100-99-4 MDL No. :MFCD20269640
Formula : C9H10BrN Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 212.09 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 162100-99-4 ]

* 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 [ 162100-99-4 ]

[ 162100-99-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 248602-16-6 ]
  • [ 162100-99-4 ]
YieldReaction ConditionsOperation in experiment
With sodium cyanoborohydride; acetic acid; at -10 - 20℃; Steps 1-3 A solution of <strong>[248602-16-6]6-bromo-5-methylindole</strong> (1.00 g, 4.75 mmol) in AcOH (150 mL) was treated with NaBH3CN (0.897 g, 14.3 mmol) while maintaining a temperature of -10 C. The mixture was then stirred at RT overnight and concentrated. The resulting residue was treated with aqueous K2CO3, and extracted with DCM (3×100 mL). The combined organic layers were dried over MgSO4, concentrated and purified by column chromatography (0-75% EtOAc/hexanes) to afford 6-bromo-5-methylindoline (13A, 716 mg).
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