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Chemical Structure| 66003-50-7 Chemical Structure| 66003-50-7

Structure of 66003-50-7

Chemical Structure| 66003-50-7

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Product Details of [ 66003-50-7 ]

CAS No. :66003-50-7
Formula : C9H8O4
M.W : 180.16
SMILES Code : CC(C1=C(O)C=C(OCO2)C2=C1)=O
MDL No. :MFCD09864085

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Application In Synthesis of [ 66003-50-7 ]

* 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 [ 66003-50-7 ]

[ 66003-50-7 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 66003-50-7 ]
  • [ 1818-27-5 ]
YieldReaction ConditionsOperation in experiment
66.9% With trichlorosilane; In chlorobenzene; at 20℃; for 24h;Inert atmosphere; Compound 2 (4 g, 19.03 mmol) was dissolved in chlorobenzene (20 mL) at room temperature, protected with nitrogen, and trichlorosilane (6.6 g 49.47 mmol) was slowly added dropwise; the mixture was heated at reflux for one day and the chlorobenzene was separated by rotary evaporation. The mixture was dissolved in ImoL/L hydrochloric acid (50 mL), extracted with ethyl acetate, and after-treated, and was purified by silica gel column chromatography to give a pale yellow solid 3 (2.1 g, 12.7 mmol). The yield was 66.9%.
 

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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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