http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3966768-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_af99df08b153738cd418446a75d09bfc
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D321-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D321-06
filingDate 1973-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1976-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b976f0373350c5f822cb54bfe956f183
publicationDate 1976-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3966768-A
titleOfInvention Substituted 1,3-dioxepins
abstract The present invention is directed to new substituted 1,3-dioxepin compounds corresponding to the formula: ##SPC1## n Wherein R is a lower alkyl group of from 1 to about 8, both inclusive, carbon atoms or an aryl group of from 6 to about 8 carbon atoms inclusive. R' is hydrogen or an alkyl group of from 1 to about 8, both inclusive, carbon atoms, and n is an integer of from 0 to about 8. The present invention is further directed to a novel process for the preparation of such substituted 1,3-dioxepin compounds wherein n is 0 by reacting, at room temperatures, a corresponding trialkyl orthoalkanoate with cis-2-butene-1,4-diol in the presence of a non-oxidizing acid catalyst. The compounds of the present invention are suitable for use as herbicides.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5116402-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4707302-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5139793-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0190568-A1
priorityDate 1971-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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