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Chemical Structure| 17771-33-4 Chemical Structure| 17771-33-4

Structure of 17771-33-4

Chemical Structure| 17771-33-4

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Product Details of [ 17771-33-4 ]

CAS No. :17771-33-4
Formula : C11H12O3
M.W : 192.21
SMILES Code : O=C1CC(C)(C)OC2=C1C=CC(O)=C2
MDL No. :MFCD00100268

Safety of [ 17771-33-4 ]

Application In Synthesis of [ 17771-33-4 ]

* 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 [ 17771-33-4 ]

[ 17771-33-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17771-33-4 ]
  • [ 17329-87-2 ]
  • 2-((2,2-dimethyl-4-oxochroman-7-yl)oxy)-N-(4-nitrophenyl)acetamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
46% With potassium carbonate; In N,N-dimethyl-formamide;Heating; General procedure: A solution of 4 (150mg, 0.50mmol) in DMF (10mL), K2CO3 (140mg, 1.00mmol) and corresponding alkylamine (0.75mmol) were added. The solution was stirred at 78C for 6h. Upon completion, the reaction mixture was poured in water (40mL) and extracted with DCM, washed with brine, and the solvent was removed under vacuum. The residue was purified by flash column chromatography (DCM/MeOH) to afford the desired compounds.
 

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Technical Information

• 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 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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