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Chemical Structure| 884855-67-8 Chemical Structure| 884855-67-8

Structure of 884855-67-8

Chemical Structure| 884855-67-8

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Product Details of [ 884855-67-8 ]

CAS No. :884855-67-8
Formula : C9H6BrNO2
M.W : 240.05
SMILES Code : O=C1N(C)C2=C(C(Br)=CC=C2)C1=O
MDL No. :MFCD11147926

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Application In Synthesis of [ 884855-67-8 ]

* 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 [ 884855-67-8 ]

[ 884855-67-8 ] Synthesis Path-Downstream   1~2

  • 1
  • C9H8BrNO2 [ No CAS ]
  • [ 884855-67-8 ]
  • [ 667463-64-1 ]
  • 2
  • C9H10BrNO2 [ No CAS ]
  • [ 884855-67-8 ]
  • [ 667463-64-1 ]
YieldReaction ConditionsOperation in experiment
34.7%; 45.2% With ruthenium trichloride; dimethyl sulfoxide; at 100℃; for 5h; General procedure: A mixture of alpha-hydroxy amides 1 (1 mmol) and RuCl3 (1 mmol) were added in 2 mL DMSO and then stirred under air at 100 C for 5 h. After the completion of the reaction (monitored by TLC), the mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate (10 mLx3). The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and the solvent was evaporated to dryness. The crude residue was purified by flash chromatography on silica (petroleum ether/ethyl acetate) to afford pure isatins 2 as a red solid.
31.7%; 44.3% With dihydrogen peroxide; In dimethyl sulfoxide; at 100℃; for 3h;Green chemistry; General procedure: A mixture of alpha-hydroxy amides 1 (1 mmol) and 30% H2O2 (6 mmol) were added in 2 mlDMSO and then stirred under air at 100 oC for 3h. After the completion of the reaction (monitoredby TLC), the mixture was cooled to room temperature, diluted with water and extracted with ethylacetate (10 ml x 3). The organic layer was washed with saturated brine, dried over anhydroussodium sulfate and the solvent was evaporated to dryness. The crude residue was purified by flashchromatography on silica (PE/EA=10/1) to afford pure isatins 2 as a red solid.
 

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Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Chan-Lam Coupling Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Dihalides • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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