Home Chemistry Organometallic Reagents Organoborons 2-(3-Cyclopropylphenyl)-1,3,2-Dioxaborolane
Suzuki-Miyaura Cross-Coupling: This is the most common and important reaction for compounds like 2-(3-cyclopropylphenyl)-1,3,2-dioxaborolane. It involves coupling the boron-containing compound with an aryl or vinyl halide in the presence of a palladium catalyst and a base to form a new carbon-carbon bond.
Borylation: You can use 2-(3-cyclopropylphenyl)-1,3,2-dioxaborolane as a boron source to introduce boron functionality into other organic molecules. This can be done under various conditions, including using base and a suitable halogenating agent.
Protodeboronation: Under certain conditions, the boron atom in the dioxaborolane can be replaced with a hydrogen atom, typically in the presence of an acid or another proton source. This can be useful for further derivatization of the compound.
Halogenation: You can perform halogenation reactions with 2-(3-cyclopropylphenyl)-1,3,2-dioxaborolane to introduce different halogen substituents on the cyclopropylphenyl group.
Hydrogenation: You can hydrogenate the double bond in the dioxaborolane to obtain the corresponding saturated compound.
Grignard Reaction: You can react 2-(3-cyclopropylphenyl)-1,3,2-dioxaborolane with a Grignard reagent to form a new carbon-carbon bond.
Oxidation: You can oxidize the boron-containing compound to convert it into other functional groups.
Pd-Catalyzed Buchwald-Hartwig Amination: This reaction involves coupling the boron compound with an amine in the presence of a palladium catalyst and a base to form an amide or other nitrogen-containing compounds.
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2-(3-Cyclopropyl-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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1-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarbonitrile
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1-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropane-1-carboxylic acid
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2-(3-Cyclopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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tert-Butyl (1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate
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