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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2a819eda0adf22936a52362eeebb9fb4
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_67d3137d0c270423982b30164390d68c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F5-025
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F5-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F5-02
filingDate 2012-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb559e97bb2e464ef48977318b547378
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_486e3eb585ffb067a61ef20597b57f0d
publicationDate 2016-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9243004-B2
titleOfInvention Synthesis of boronic esters and boronic acids using grignard reagents
abstract Boronic esters and boronic acids are synthesized at ambient temperature in an ethereal solvent by the reaction of Grignard reagents with a boron-containing substrate. The boron-containing substrate may be a boronic ester such as pinacolborane, neopentylglycolborane, or a dialkylaminoborane compound such as diisopropylaminoborane. The Grignard reagents may be pre-formed or generated from an alkyl, alkenyl, aryl, arylalkyl, heteroaryl, vinyl, or allyl halide compound and Mg 0 . When the boron-containing substrate is a boronic ester, the reactions generally proceed at room temperature without added base in about 1 to 3 hours to form a boronic ester compound. When the boron-containing substrate is a dialkylaminoborane compound, the reactions generally proceed to completion at 0° C. in about 1 hour to form a boronic acid compound.
priorityDate 2011-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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