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Chemical Structure| 29124-64-9 Chemical Structure| 29124-64-9

Structure of 29124-64-9

Chemical Structure| 29124-64-9

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Product Details of [ 29124-64-9 ]

CAS No. :29124-64-9
Formula : C10H10BrNO2
M.W : 256.10
SMILES Code : CC(=O)NC1=C(C=C(Br)C=C1)C(C)=O
MDL No. :MFCD00460457

Safety of [ 29124-64-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 29124-64-9 ]

* 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 [ 29124-64-9 ]

[ 29124-64-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5234-26-4 ]
  • [ 29124-64-9 ]
YieldReaction ConditionsOperation in experiment
89% With bromine; In diethyl ether; acetic acid; Example 34B N-(2-acetyl-4-bromophenyl)acetamide A solution Example 34A (6.5 g, 37 mmol) in acetic acid (100 mL) at room temperature was treated with Br2 (4 mL, 84 mmol), stirred for 1 hour and 15 minutes, poured into water (200 mL), and filtered. The solid was washed with water (2*100 mL), and hexanes (2*100 mL), dissolved in diethyl ether, washed with brine (50 mL), and concentrated to provide the desired product (8.5 g, 89%).
89% With bromine; In acetic acid; at 20℃; for 1.25h; Example 34B N-(2-acetyl-4-bromophenyl)acetamide A solution Example 34A (6.5 g, 37 mmol) in acetic acid (100 mL) at room temperature was treated with Br2 (4 mL, 84 mmol), stirred for 1 hour and 15 minutes, poured into water (200 mL), and filtered. The solid was washed with water (2*100 mL), and hexanes (2*100 mL), dissolved in diethyl ether, washed with brine (50 mL), and concentrated to provide the desired product (8.5 g, 89%).
89% With bromine; acetic acid; at 20℃; for 2h; N- (2-acetylphenyl) acetamide (2.66 g, 14.8 mmol)In acetic acid (40 mL), bromine (1.52 mL, 29.6 mmol) was added and the mixture was stirred at room temperature for 2 hours. The reaction solution was poured into water,Precipitates were collected by filtration. The resulting solid was washed with water and hexane to give the title compound (3.37 g, 89%). Light yellow solid
86% With bromine; In acetic acid; at 20℃; for 2.33333h;Inert atmosphere; Under N2, a pale yellow suspension of crude <strong>[5234-26-4]N-(2-acetylphenyl)acetamide</strong>(28 g, 158 mmol) in AcOH (300 mL) was stirred for about 5 min, and Br2 (12.95 mL, 253 mmol) was added within 1 h at room temperature. The resulting mixture was then stirred at room temperature for 75 min. After the reaction went to completion as monitored by LC-MS, the reaction mixture was quenched with H2O (200 mL). The mixture was filtered through Buchner funnel, and the solid was collected as N-(2- acetyl-4-bromophenyl)acetamide (35g, yield 86%). MS (m/z): 216 (M+H)+.
86% With bromine; In acetic acid; at 20℃; for 2.33333h;Inert atmosphere; Under N2, a pale yellow suspension of crude <strong>[5234-26-4]N-(2-acetylphenyl)acetamide</strong> (28 g, 158 mmol) in AcOH (300 mL) was stirred for about 5 min, and Br2 (12.95 mL, 253 mmol) was added within 1 h at room temperature. The resulting mixture was then stirred at room temperature for 75 min. After the reaction went to completion as monitored by LC-MS, the reaction mixture was quenched with H2O (200 mL). The mixture was filtered through Buchner funnel, and the solid was collected as N-(2-acetyl-4-bromophenyl)acetamide (35 g, yield 86%). MS (m/z): 216 (M+H)+.

 

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Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • 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 • Mannich 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 • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • 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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