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Chemical Structure| 53811-50-0 Chemical Structure| 53811-50-0

Structure of 53811-50-0

Chemical Structure| 53811-50-0

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Product Details of [ 53811-50-0 ]

CAS No. :53811-50-0
Formula : C9H9BrO3
M.W : 245.07
SMILES Code : O=CC1=C(Br)C=CC(OC)=C1OC
MDL No. :MFCD03414707

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Application In Synthesis of [ 53811-50-0 ]

* 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 [ 53811-50-0 ]

[ 53811-50-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 53811-50-0 ]
  • [ 6880-91-7 ]
  • 2
  • [ 53811-50-0 ]
  • [ 2934-97-6 ]
  • 3
  • [ 53811-50-0 ]
  • [ 6299-67-8 ]
  • N-(6-bromo-2,3-dimethoxybenzyl)-2,3-dimethoxyaniline [ No CAS ]
YieldReaction ConditionsOperation in experiment
34% With sodium tris(acetoxy)borohydride; In toluene; at 20℃; for 1h; General procedure: To a solution of bromobenzaldehyde 2b(1.0 g; 4.08 mmol) and aniline 1a (644 mg; 4.20 mmol) in anhydrous toluene (50 mL) was addedNaBH(OAc)3 (2.6 g; 12.2 mmol). The resulting suspension was stirred at room temperature for 1 h,and then washed with water (2 x 35 mL) and brine (1 x 40 mL). The aqueous phase was extracted withtoluene (1 x 40 mL). The combined organic extracts were dried over Na2SO4, filtered and concentratedunder reduced pressure. To induce crystallization of the product, MeOH (8 mL) was added to theresidue. The resulting solid was filtered off, washed with cold MeOH (1 mL) and dried. Compound4e was obtained as a slightly pink crystalline solid (1.19 g; 76%).Mp. = 79-80 C;
 

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• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Julia-Kocienski Olefination • Kinetics of Alkyl Halides • Knoevenagel Condensation • Kumada Cross-Coupling Reaction • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nomenclature of Ethers • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Ethers • 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 of Ethers • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Stetter Reaction • 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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