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Chemical Structure| 121612-23-5 Chemical Structure| 121612-23-5

Structure of 121612-23-5

Chemical Structure| 121612-23-5

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Product Details of [ 121612-23-5 ]

CAS No. :121612-23-5
Formula : C9H10O2
M.W : 150.17
SMILES Code : CC1=CC(C(CO)=O)=CC=C1
MDL No. :MFCD16165843

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Application In Synthesis of [ 121612-23-5 ]

* 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 [ 121612-23-5 ]

[ 121612-23-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 51012-64-7 ]
  • [ 121612-23-5 ]
YieldReaction ConditionsOperation in experiment
With water; In acetonitrile; at 125℃; for 0.833333h; Step 2: 2-hydroxy-l-(3-methylphenyl)ethanone; [00340] A solution of 2-bromo- 1 -(3 -methylphenyl)ethanone (1 g) in acetonitrile (2.5 mL) and water (13 mL) is treated under microwave irradiation (125C, 50 min). The same experiment is repeated three times. All the vials are collected, extracted with DCM, dried over magnesium sulfate and concentrated under vacuum to give the desired compound.TLC: Fr = 0.15 (ethyl acetate/cyclohexane : 10/90). delta 1H NMR (CDCl3): 2.47 (s, 3H); 4.90 (s, 2H); 7.41-7.49 (m, 2H); 7.74-7.78 (m, 2H).
29 g With water; sodium hydroxide; In ethanol; for 20h;Reflux; 50 g of 2-bromo-1-(3-methylphenyl)ethanone was added to 600 ml of ethanol, 100 ml of water and 80 g of sodium hydroxide were added, and the mixture was heated under reflux for 20 hours, cooled, concentrated, and then added with ethyl acetate to separate the liquid. After drying and concentrating, the residue was separated by column to give 29 g of 1-(3-methylphenyl)-2-hydroxyethanone.
  • 2
  • [ 51012-64-7 ]
  • [ 1157136-21-4 ]
  • [ 121612-23-5 ]
 

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• Appel Reaction • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Grignard Reaction • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Lawesson's Reagent • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Alcohols • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Alcohols • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Specialized Acylation Reagents-Ketenes • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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