Methods of forming 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol esters and methods of using the same
AssigneeDow AgroSciences LLC
InventorJossian MI Oppenheimer
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AssigneeDow AgroSciences LLC
InventorJossian MI Oppenheimer
Estimating the term…
Methods include formation of 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol esters. The method comprises contacting a 1-chloro-3-fluoro-2-substituted benzene with an alkyl lithium to form a lithiated 1-chloro-3-fluoro-2-substituted benzene. The lithiated 1-chloro-3-fluoro-2-substituted benzene is contacted with an electrophilic boronic acid derivative to form a 4-chloro-2-fluoro-3-substituted-phenylboronate. The 4-chloro-2-fluoro-3-substituted-phenylboronate is reacted with an aqueous base to form a (4-chloro-2-fluoro-3-substituted-phenyl)trihydroxyborate. The (4-chloro-2-fluoro-3-substituted-phenyl)trihydroxyborate is reacted with an acid to form a 4 chloro-2-fluoro-3-substituted-phenylboronic acid. The 4-chloro-2-fluoro-3-substituted-phenylboronic acid is reacted with 2,3-dimethyl-2,3-butanediol to form 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol esters. Methods of using 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol esters to produce 6-(4-chloro-2-fluoro-3-substituted-phenyl)-4-aminopicolinates are also disclosed.
A method of forming a 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol ester, comprising:
A method of forming 2-(4-chloro-2-fluoro-3-methoxylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, comprising:
A method of using a 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol ester comprising reacting the 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol ester with methyl 4-acetamido-3,6-dichloropicolinate to produce a 6-(4-chloro-2-fluoro-3-substituted-phenyl)-4-aminopicolinate.
A 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol ester produced by introducing 2,3-dimethyl-2,3-butanediol into a solution comprising a 4-chloro-2-fluoro-3-substituted-phenylboronic acid, wherein the 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol ester is obtained at a yield of greater than approximately 90%.
Dependencies are inferred from the claim text.