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Chemical Structure| 51765-77-6 Chemical Structure| 51765-77-6

Structure of 51765-77-6

Chemical Structure| 51765-77-6

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Product Details of [ 51765-77-6 ]

CAS No. :51765-77-6
Formula : C10H8BrNO
M.W : 238.08
SMILES Code : N#CCCC(C1=CC=C(Br)C=C1)=O
MDL No. :MFCD02260543

Safety of [ 51765-77-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330-P501

Application In Synthesis of [ 51765-77-6 ]

* 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 [ 51765-77-6 ]

[ 51765-77-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 773837-37-9 ]
  • [ 31736-73-9 ]
  • [ 51765-77-6 ]
YieldReaction ConditionsOperation in experiment
31.8% At 70 C, To a solution of 4'-bromo-3-chlorophenylacetone (1 g, 4 mmol) in ethyl acetate (30 mL) was added potassium tert-butoxide (453 mg, 4 mmol) and the reaction was allowed to proceed for 15 minutes and then cooled to room temperature.The solids were removed by filtration and the filtrate was collected.A solution of sodium cyanide (396 mg, 8 mmol) in water (30 mL) was slowly added dropwise to the resulting solution (dropwise over 30 minutes), and the stirring was continued for 30 minutes after completion of the addition.Ethanol (20 mL) was added and stirring was continued for 3 hours.The organic phase was separated, concentrated and chromatographed (petroleum ether: ethyl acetate = 10: 1) to give the title compound (306 mg, 31.8%).
 

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• Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Blaise Reaction • Bucherer-Bergs Reaction • Catalytic Hydrogenation • 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 Benzene and Substituted Benzenes • Reactions of Dihalides • Reformatsky Reaction • Ritter Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Thorpe-Ziegler Reaction • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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