The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 29, 2015

Filed:

Sep. 14, 2012
Applicants:

Mark V. M. Emonds, Midland, MI (US);

Catherine A. Menning, Midland, MI (US);

D. Wayne Blaylock, Midland, MI (US);

Inventors:

Mark V. M. Emonds, Midland, MI (US);

Catherine A. Menning, Midland, MI (US);

D. Wayne Blaylock, Midland, MI (US);

Assignee:

Dow AgroSciences LLC, Indianapolis, IN (US);

Attorneys:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C07F 5/04 (2006.01); C07F 5/02 (2006.01); B01J 19/00 (2006.01); B01J 19/24 (2006.01);
U.S. Cl.
CPC ...
C07F 5/025 (2013.01); B01J 19/0093 (2013.01); B01J 19/24 (2013.01); B01J 2219/0004 (2013.01); B01J 2219/00011 (2013.01); B01J 2219/0086 (2013.01); B01J 2219/00094 (2013.01); B01J 2219/00099 (2013.01); B01J 2219/00795 (2013.01); B01J 2219/00813 (2013.01); B01J 2219/00822 (2013.01); B01J 2219/00867 (2013.01); B01J 2219/00873 (2013.01); B01J 2219/00894 (2013.01);
Abstract

Methods for forming boronic acids, and intermediates thereof, are disclosed. The method may include mixing a 1-chloro-2-substituted-3-fluorobenzene starting material with an alkyllithium in a first reactor to form a reaction mixture. The 1-chloro-2-substituted-3-fluorobenzene starting material may react with the alkyllithium to form a lithiated intermediate. The reaction mixture may be continuously transferred to a second reactor and a borate may be continuously introduced to form a boronate. The boronic acids may be formed by treating the boronate with aqueous potassium hydroxide followed by acidification. Such methods may provide continuous formation of the boronic acids and may reduce an amount of a reactive intermediate present during processing as well as cycle times. Systems for forming the boronic acids are also disclosed.


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