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Chemical Structure| 133993-34-7 Chemical Structure| 133993-34-7

Structure of 133993-34-7

Chemical Structure| 133993-34-7

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Product Details of [ 133993-34-7 ]

CAS No. :133993-34-7
Formula : C11H11BrO3
M.W : 271.11
SMILES Code : CCOC(=O)C1=C(C=CC=C1)C(=O)CBr
MDL No. :MFCD00142009
InChI Key :RVUDSNUPKXBRKT-UHFFFAOYSA-N
Pubchem ID :2764121

Safety of [ 133993-34-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P280-P305+P351+P338-P310

Application In Synthesis of [ 133993-34-7 ]

* 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 [ 133993-34-7 ]

[ 133993-34-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 103935-10-0 ]
  • [ 133993-34-7 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; toluene-4-sulfonic acid; In acetonitrile; at 50℃; for 6h; A mixture of ethyl2-(2-bromoacetyl)benzoate (53 mg, 0.26 mmol, 1 eq), N-bromosuccinimide ( 48mg, 0.27 mmol, 1.02 eq) and p-TsOH.H20 (50 mg, 0.26 mmol, 1 eq) in acetonitrile (140.0 JlL) is stirred at50C for 6 h. The reaction mixture is diluted (ethyl acetate), washed (saturated NaHC03 and brine), dried(Na2S04) and concentrated. The residue is purified by flash column chromatography (Si02,cyclohexane/DCM 100:0 to 20:80) to afford the desired product.
 

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Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bouveault-Blanc Reduction • Bucherer-Bergs Reaction • Catalytic Hydrogenation • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Ester Cleavage • 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 • Reactions with Organometallic Reagents • 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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